Temazepam Civ (Temazepam)

Trade Name : temazepam

NuCare Pharmaceuticals,Inc.

CAPSULE

Strength 30 mg/1

TEMAZEPAM Benzodiazepine [EPC],Benzodiazepines [CS]

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Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Temazepam Civ (Temazepam) which is also known as temazepam and Manufactured by NuCare Pharmaceuticals,Inc.. It is available in strength of 30 mg/1 per ml. Read more

Temazepam Civ (Temazepam) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials. Click to know price. Read less

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Temazepam is a benzodiazepine hypnotic agent. The chemical name is 7-chloro-1,3-dihydro-3-hydroxy-1-methyl-5-phenyl-2H-1, 4-benzodiazepin-2-one, and the structural formula is:
Cn n n Hn n n ClNn n n On n n MW = 300.74n n n n Temazepam is a white, crystalline substance, very slightly soluble in water and sparingly soluble in alcohol USP. n nn
Temazepam capsules, 7.5 mg, 15 mg, 22.5 mg and 30 mg, are for oral administration.n n n n n Active Ingredient: temazepam USPn n n n n Corn starch, lactose anhydrous, magnesium stearate, sodium lauryl sulfate, FD&C Red #40 and titanium dioxide.n nn
May also include:
Arrayn- 15 mg Capsules
Inactive Ingredients:
May also include:
Arrayn- 22.5 mg Capsules
Inactive Ingredients:
May also include:
Arrayn- 30 mg Capsules
Inactive Ingredients:
May also include:

Pharmacokinetics
In a single and multiple dose absorption, distribution, metabolism, and excretion (ADME) study, using 3H labeled drug, temazepam was well absorbed and found to have minimal (8%) first pass metabolism. There were no active metabolites formed and the only significant metabolite present in blood was the O-conjugate. The unchanged drug was 96% bound to plasma proteins. The blood level decline of the parent drug was biphasic with the short half-life ranging from 0.4 to 0.6 hours and the terminal half-life from 3.5 to 18.4 hours (mean 8.8 hours), depending on the study population and method of determination. Metabolites were formed with a half-life of 10 hours and excreted with a half-life of approximately 2 hours. Thus, formation of the major metabolite is the rate limiting step in the biodisposition of temazepam. There is no accumulation of metabolites. A dose-proportional relationship has been established for the area under the plasma concentration/time curve over the 15 to 30 mg dose range.
Temazepam was completely metabolized through conjugation prior to excretion; 80% to 90% of the dose appeared in the urine. The major metabolite was the O-conjugate of temazepam (90%); the O-conjugate of N-desmethyl temazepam was a minor metabolite (7%).
Bioavailability, Induction, and Plasma Levels
Following ingestion of a 30 mg temazepam capsule, measurable plasma concentrations were achieved 10 to 20 minutes after dosing with peak plasma levels ranging from 666 to 982 ng/mL (mean 865 ng/mL) occurring approximately 1.2 to 1.6 hours (mean 1.5 hours) after dosing.
In a 7 day study, in which subjects were given a 30 mg temazepam capsule 1 hour before retiring, steady-state (as measured by the attainment of maximal trough concentrations) was achieved by the third dose. Mean plasma levels of temazepam (for days 2 to 7) were 260u00b1210 ng/mL at 9 hours and 75u00b180 ng/mL at 24 hours after dosing. A slight trend toward declining 24 hour plasma levels was seen after day 4 in the study, however, the 24 hour plasma levels were quite variable.
At a dose of 30 mg once-a-day for 8 weeks, no evidence of enzyme induction was found in man.
Elimination Rate of Benzodiazepine Hypnotics and Profile of Common Untoward Effects
The type and duration of hypnotic effects and the profile of unwanted effects during administration of benzodiazepine hypnotics may be influenced by the biologic half-life of the administered drug and for some hypnotics, the half-life of any active metabolites formed. Benzodiazepine hypnotics have a spectrum of half-lives from short (<4 hours) to long (>20 hours). When half-lives are long, drug (and for some drugs their active metabolites) may accumulate during periods of nightly administration and be associated with impairments of cognitive and/or motor performance during waking hours; the possibility of interaction with other psychoactive drugs or alcohol will be enhanced. In contrast, if half-lives are shorter, drug (and, where appropriate, its active metabolites) will be cleared before the next dose is ingested, and carry-over effects related to excessive sedation or CNS depression should be minimal or absent. However, during nightly use for an extended period, pharmacodynamic tolerance or adaptation to some effects of benzodiazepine hypnotics may develop. If the drug has a short elimination half-life, it is possible that a relative deficiency of the drug, or, if appropriate, its active metabolites (i.e., in relationship to the receptor site) may occur at some point in the interval between each nightu2019s use. This sequence of events may account for 2 clinical findings reported to occur after several weeks of nightly use of rapidly eliminated benzodiazepine hypnotics, namely, increased wakefulness during the last third of the night, and the appearance of increased signs of daytime anxiety.
Controlled Trials Supporting Efficacy
Temazepam improved sleep parameters in clinical studies. Residual medication effects (u201changoveru201d) were essentially absent. Early morning awakening, a particular problem in the geriatric patient, was significantly reduced.
Patients with chronic insomnia were evaluated in 2 week, placebo controlled sleep laboratory studies with temazepam at doses of 7.5 mg, 15 mg, and 30 mg, given 30 minutes prior to bedtime. There was a linear dose-response improvement in total sleep time and sleep latency, with significant drug-placebo differences at 2 weeks occurring only for total sleep time at the 2 higher doses, and for sleep latency only at the highest dose.
In these sleep laboratory studies, REM sleep was essentially unchanged and slow wave sleep was decreased. No measurable effects on daytime alertness or performance occurred following temazepam treatment or during the withdrawal period, even though a transient sleep disturbance in some sleep parameters was observed following withdrawal of the higher doses. There was no evidence of tolerance development in the sleep laboratory parameters when patients were given temazepam nightly for at least 2 weeks.
In addition, normal subjects with transient insomnia associated with first night adaptation to the sleep laboratory were evaluated in 24 hour, placebo controlled sleep laboratory studies with temazepam at doses of 7.5 mg, 15 mg, and 30 mg, given 30 minutes prior to bedtime. There was a linear dose-response improvement in total sleep time, sleep latency and number of awakenings, with significant drug-placebo differences occurring for sleep latency at all doses, for total sleep time at the 2 higher doses and for number of awakenings only at the 30 mg dose.

Temazepam Capsules, USP are indicated for the short-term treatment of insomnia (generally 7 to 10 days). For patients with short-term insomnia, instructions in the prescription should indicate that Temazepam Capsules should be used for short periods of time (7 to 10 days).
The clinical trials performed in support of efficacy were 2 weeks in duration with the final formal assessment of sleep latency performed at the end of treatment.

Benzodiazepines may cause fetal harm when administered to a pregnant woman. An increased risk of congenital malformations associated with the use of diazepam and chlordiazepoxide during the first trimester of pregnancy has been suggested in several studies. Transplacental distribution has resulted in neonatal CNS depression following the ingestion of therapeutic doses of a benzodiazepine hypnotic during the last weeks of pregnancy.
Reproduction studies in animals with temazepam were performed in rats and rabbits. In a perinatal-postnatal study in rats, oral doses of 60 mg/kg/day resulted in increasing nursling mortality. Teratology studies in rats demonstrated increased fetal resorptions at doses of 30 and 120 mg/kg in one study and increased occurrence of rudimentary ribs, which are considered skeletal variants, in a second study at doses of 240 mg/kg or higher. In rabbits, occasional abnormalities such as exencephaly and fusion or asymmetry of ribs were reported without dose relationship. Although these abnormalities were not found in the concurrent control group, they have been reported to occur randomly in historical controls. At doses of 40 mg/kg or higher, there was an increased incidence of the 13th rib variant when compared to the incidence in concurrent and historical controls.
Temazepam is contraindicated in women who are or may become pregnant. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus. Patients should be instructed to discontinue the drug prior to becoming pregnant. The possibility that a woman of childbearing potential may be pregnant at the time of institution of therapy should be considered.

Sleep disturbance may be the presenting manifestation of an underlying physical and/or psychiatric disorder. Consequently, a decision to initiate symptomatic treatment of insomnia should only be made after the patient has been carefully evaluated. n n n Worsening of insomnia may be the consequence of an unrecognized psychiatric or physical disorder as may the emergence of new abnormalities of thinking or behavior. Such abnormalities have also been reported to occur in association with the use of drugs with central nervous system depressant activity, including those of the benzodiazepine class. Because some of the worrisome adverse effects of benzodiazepines, including temazepam, appear to be dose related (n n n n n n ), it is important to use the lowest possible effective dose.Elderly patients are especially at risk.n nn
Some of these changes may be characterized by decreased inhibition, e.g., aggressiveness and extroversion that seem out of character, similar to that seen with alcohol. Other kinds of behavioral changes can also occur, for example, bizarre behavior, agitation, hallucinations, and depersonalization. Complex behaviors such as u201csleep-drivingu201d (i.e., driving while not fully awake after ingestion of a sedative-hypnotic, with amnesia for the event) have been reported. These events can occur in sedative-hypnotic-nau00efve as well as in sedative-hypnotic-experienced persons. Although behaviors such as sleep-driving may occur with temazepam alone at therapeutic doses, the use of alcohol and other CNS depressants with temazepam appears to increase the risk of such behaviors, as does the use of temazepam at doses exceeding the maximum recommended dose. Due to the risk to the patient and the community, discontinuation of temazepam should be strongly considered for patients who report a u201csleep-drivingu201d episode. Other complex behaviors (e.g., preparing and eating food, making phone calls, or having sex) have been reported in patients who are not fully awake after taking a sedative-hypnotic. As with sleep-driving, patients usually do not remember these events. Amnesia and other neuro-psychiatric symptoms may occur unpredictably. In primarily depressed patients, worsening of depression, including suicidal thinking has been reported in association with the use of sedative/hypnotics.
It can rarely be determined with certainty whether a particular instance of the abnormal behaviors listed above is drug induced, spontaneous in origin, or a result of an underlying psychiatric or physical disorder. Nonetheless, the emergence of any new behavioral sign or symptom of concern requires careful and immediate evaluation.
Withdrawal symptoms (of the barbiturate type) have occurred after the abrupt discontinuation of benzodiazepines (n n n n ).n nn
Severe Anaphylactic and Anaphylactoid Reactions
Rare cases of angioedema involving the tongue, glottis or larynx have been reported in patients after taking the first or subsequent doses of sedative-hypnotics, including temazepam. Some patients have had additional symptoms such as dyspnea, throat closing, or nausea and vomiting that suggest anaphylaxis. Some patients have required medical therapy in the emergency department. If angioedema involves the tongue, glottis or larynx, airway obstruction may occur and be fatal. Patients who develop angioedema after treatment with temazepam should not be rechallenged with the drug.u00a0

No data

During controlled clinical studies in which 1076 patients received temazepam at bedtime, the drug was well tolerated. Side effects were usually mild and transient. Adverse reactions occurring in 1% or more of patients are presented in the following table:
The following adverse events have been reported less frequently (0.5% to 0.9%):
Central Nervous System
Cardiovascular n- Gastrointestinal
Musculoskeletal
Special Senses
Amnesia, hallucinations, horizontal nystagmus, and paradoxical reactions including restlessness, overstimulation and agitation were rare (less than 0.5%).

Abuse and addiction are separate and distinct from physical dependence and tolerance. Abuse is characterized by misuse of the drug for non-medical purposes, often in combination with other psychoactive substances. Physical dependence is a state of adaptation that is manifested by a specific withdrawal syndrome that can be produced by abrupt cessation, rapid dose reduction, decreasing blood level of the drug and/or administration of an antagonist. Tolerance is a state of adaptation in which exposure to a drug induces changes that result in a diminution of one or more of the drugu2019s effects over time. Tolerance may occur to both the desired and undesired effects of drugs and may develop at different rates for different effects.
Addiction is a primary, chronic, neurobiological disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. It is characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving. Drug addiction is a treatable disease, utilizing a multidisciplinary approach, but relapse is common.
Controlled Substance
Temazepam is a controlled substance in Schedule IV.
Abuse and Dependence
Withdrawal symptoms, similar in character to those noted with barbiturates and alcohol (convulsions, tremor, abdominal, and muscle cramps, vomiting, and sweating), have occurred following abrupt discontinuance of benzodiazepines. The more severe withdrawal symptoms have usually been limited to those patients who received excessive doses over an extended period of time. Generally milder withdrawal symptoms (e.g., dysphoria and insomnia) have been reported following abrupt discontinuance of benzodiazepines taken continuously at therapeutic levels for several months. Consequently, after extended therapy at doses higher than 15 mg, abrupt discontinuation should generally be avoided and a gradual dosage tapering schedule followed. As with any hypnotic, caution must be exercised in administering temazepam to individuals known to be addiction-prone or to those whose history suggests they may increase the dosage on their own initiative. It is desirable to limit repeated prescriptions without adequate medical supervision.

Manifestations of acute overdosage of temazepam can be expected to reflect the CNS effects of the drug and include somnolence, confusion, and coma, with reduced or absent reflexes, respiratory depression, and hypotension. The oral LD50 of temazepam was 1963 mg/kg in mice, 1833 mg/kg in rats, and >2400 mg/kg in rabbits.
Treatment
If the patient is conscious, vomiting should be induced mechanically or with emetics. Gastric lavage should be employed utilizing concurrently a cuffed endotracheal tube if the patient is unconscious to prevent aspiration and pulmonary complications. Maintenance of adequate pulmonary ventilation is essential. The use of pressor agents intravenously may be necessary to combat hypotension. Fluids should be administered intravenously to encourage diuresis. The value of dialysis has not been determined. If excitation occurs, barbiturates should not be used. It should be borne in mind that multiple agents may have been ingested. Flumazenil (Romaziconu00ae)*, a specific benzodiazepine receptor antagonist, is indicated for the complete or partial reversal of the sedative effects of benzodiazepines and may be used in situations when an overdose with a benzodiazepine is known or suspected. Prior to the administration of flumazenil, necessary measures should be instituted to secure airway, ventilation, and intravenous access. Flumazenil is intended as an adjunct to, not as a substitute for, proper management of benzodiazepine overdose. Patients treated with flumazenil should be monitored for re-sedation, respiratory depression, and other residual benzodiazepine effects for an appropriate period after treatment. n n n The complete flumazenil package insert including CONTRAINDICATIONS, WARNINGS, and PRECAUTIONS should be consulted prior to use.n nn
Up-to-date information about the treatment of overdose can often be obtained from a certified Regional Poison Control Center. Telephone numbers of certified Regional Poison Control Centers are listed in the Physiciansu2019 Desk Referencesu00ae**.

While the recommended usual adult dose is 15 mg before retiring, 7.5 mg may be sufficient for some patients, and others may need 30 mg. In transient insomnia, a 7.5 mg dose may be sufficient to improve sleep latency. In elderly or debilitated patients, it is recommended that therapy be initiated with 7.5 mg until individual responses are determined.

Arrayn- 30 mg
White opaque cap and body, imprinted 30 mg on cap and Novel 123 on the body in black ink.
NDC 66267-321-30 Bottles of 30
Arrayn- Dispense in a well-closed, light-resistant container with a child-resistant closure.
Storage:
Romazicon is the registered trademark of Hoffman-LaRoche Inc.
Trademark of Medical Economics Company, Inc.
Manufactured by:
Novel Laboratories Inc.
Somerset, NJ 08873
Distributed by:
Ascend Laboratories, LLC
Parsippany, NJ 07054

TEMAZEPAM Capsules, USP CIVu00a0n n n (temazepam)n n n n
u00a0
Read the Medication Guide that comes with TEMAZEPAM before you start taking it and each time you get a refill. There may be new information. This Medication Guide does not take the place of talking to your doctor about your medical condition or treatment.
What is the most important information I should know about TEMAZEPAM?
After taking TEMAZEPAM, you may get up out of bed while not being fully awake and do an activity that you do not know you are doing. The next morning, you may not remember that you did anything during the night.
u00b7u00a0u00a0u00a0u00a0u00a0u00a0driving a car (u201csleep-drivingu201d)
u00b7u00a0u00a0u00a0u00a0u00a0u00a0making and eating food
u00b7u00a0u00a0u00a0u00a0u00a0u00a0talking on the phone
u00b7u00a0u00a0u00a0u00a0u00a0u00a0having sex
u00b7u00a0u00a0u00a0u00a0u00a0u00a0sleep-walking
Call your doctor right away if you find out that you have done any of the above activities after taking TEMAZEPAM.
Important:
1.u00a0 Take TEMAZEPAM exactly as prescribed
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Do not take more TEMAZEPAM than prescribed.
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Take TEMAZEPAM right before you get in bed, not sooner.
2.u00a0 Do not take TEMAZEPAM if you:
u00b7u00a0u00a0u00a0u00a0u00a0u00a0drink alcohol
u00b7u00a0u00a0u00a0u00a0u00a0u00a0take other medicines that can make you sleepy. Talk to your doctor about all of your medicines. Your doctor will tell you if you can take TEMAZEPAM with your other medicines
u00b7u00a0u00a0u00a0u00a0u00a0u00a0cannot get a full nightu2019s sleep
What is TEMAZEPAM?
TEMAZEPAM is a sedative-hypnotic (sleep) medicine.
TEMAZEPAM is used in adults for the short-term (usually 7 to 10 days) treatment of a sleep problem called insomnia.
Symptoms of insomnia include:
u00b7u00a0u00a0u00a0u00a0u00a0u00a0trouble falling asleep
u00b7u00a0u00a0u00a0u00a0u00a0u00a0waking up often during the night
TEMAZEPAM is not for children.
Arrayn- Array
Do not take TEMAZEPAM if you are pregnant or planning to become pregnant.
TEMAZEPAM may not be right for you. Before starting TEMAZEPAM, tell your doctor about all of your health conditions, including if you:
u00b7u00a0u00a0u00a0u00a0u00a0u00a0have a history of depression, mental illness, or suicidal thoughts
u00b7u00a0u00a0u00a0u00a0u00a0u00a0have a history of drug or alcohol abuse or addiction
u00b7u00a0u00a0u00a0u00a0u00a0u00a0have kidney or liver disease
u00b7u00a0u00a0u00a0u00a0u00a0u00a0have a lung disease or breathing problems
u00b7u00a0u00a0u00a0u00a0u00a0u00a0are breastfeeding
Tell your doctor about all of the medicines you take including prescription and nonprescription medicines, vitamins and herbal supplements. Medicines can interact with each other, sometimes causing serious side effects.u00a0n n n n
Know the medicines you take. Keep a list of your medicines with you to show your doctor and pharmacist each time you get a new medicine.
How should I take TEMAZEPAM?
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Take TEMAZEPAM exactly as prescribed. Do not take more TEMAZEPAM than prescribed for you.
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n n
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n n
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n u00a0This may mean that there is another condition causing your sleep problems.n nn
u00b7u00a0u00a0u00a0u00a0u00a0u00a0If you take too much TEMAZEPAM or overdose, call your doctor or poison control center right away, or get emergency treatment.
Arrayn- Array
Possible serious side effects of TEMAZEPAM include:
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n u00a0(See u201cWhat is the most important information I should know about TEMAZEPAM?u201d)n nn
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n u00a0Symptoms include more outgoing or aggressive behavior than normal, confusion, agitation, hallucinations, worsening of depression, and suicidal thoughts.n nn
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n n
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n n
u00b7u00a0u00a0u00a0u00a0u00a0u00a0n n n . Symptoms include swelling of the tongue or throat, trouble breathing, and nausea and vomiting. Get emergency medical help if you get these symptoms after taking TEMAZEPAM.n nn
Call your doctor right away if you have any of the above side effects or any other side effects that worry you while using TEMAZEPAM.
The most common side effects of TEMAZEPAM are:
u00b7u00a0u00a0u00a0u00a0u00a0u00a0drowsiness
u00b7u00a0u00a0u00a0u00a0u00a0u00a0headache
u00b7u00a0u00a0u00a0u00a0u00a0u00a0tiredness
u00b7u00a0u00a0u00a0u00a0u00a0u00a0nervousness
u00b7u00a0u00a0u00a0u00a0u00a0u00a0dizziness
u00b7u00a0u00a0u00a0u00a0u00a0u00a0nausea
u00b7u00a0u00a0u00a0u00a0u00a0u00a0u201changoveru201d feeling the day after taking TEMAZEPAM
u00b7u00a0u00a0u00a0u00a0u00a0u00a0You may still feel drowsy the next day after taking TEMAZEPAM.u00a0n n n .n nn
u00b7u00a0u00a0u00a0u00a0u00a0u00a0You may have withdrawal symptoms if you stop taking TEMAZEPAM suddenly. Withdrawal symptoms can be serious and include seizures. Mild withdrawal symptoms include a depressed mood and trouble sleeping. Talk to your doctor to check if you need to stop TEMAZEPAM slowly.
These are not all the side effects of TEMAZEPAM. Ask your doctor or pharmacist for more information.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
How should I store TEMAZEPAM?
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Store TEMAZEPAM at room temperature, 68u00b0 to 77u00b0F (20u00b0 to 25u00b0C).
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Keep TEMAZEPAM and all medicines out of reach of children.
General Information about TEMAZEPAM
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide.
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Do not use TEMAZEPAM for a condition for which it was not prescribed.
u00b7u00a0u00a0u00a0u00a0u00a0u00a0Do not share TEMAZEPAM with other people, even if you think they have the same symptoms that you have. It may harm them and it is against the law.
This Medication Guide summarizes the most important information about TEMAZEPAM. If you would like more information, talk with your doctor. You can ask your doctor or pharmacist for information about TEMAZEPAM that is written for healthcare professionals.
What are the ingredients in TEMAZEPAM?
Arrayn- 7.5mg, 15mg, 22.5mg and 30mg Capsules
Active Ingredient: temazepam USP
Arrayn- 7.5 mg Capsules
Inactive Ingredients:u00a0
May also include:u00a0
Arrayn- 15 mg Capsules
Inactive Ingredients:u00a0
May also include:u00a0
contain ammonium hydroxide, ethanol, isopropyl alcohol, butanol, shellac, potassium hydroxide, propylene glycol, and black iron oxide.
Arrayn- 22.5 mg Capsules
Inactive Ingredients:u00a0
May also include:u00a0
Arrayn- 30 mg Capsules
Inactive Ingredients:u00a0
May also include:u00a0
Manufactured by:
Novel Laboratories, Inc
Somerset, NJ 08873
Distributed by:
ASCEND Laboratories, LLC
Parsippany, NJ 07054
ALPI-147-05-04
Rev: 09/2017u00a0

No data

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Temazepam Civ (Temazepam)

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Temazepam Civ (Temazepam)

Trade Name : temazepam

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Product information is meant for

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

Packaging and Delivery

About GNH

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