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Diclofenac Sodium (Diclofenac Sodium)

Trade Name : Diclofenac Sodium

NuCare Pharmaceuticals,Inc.

TABLET, DELAYED RELEASE

Strength 75 mg/1

DICLOFENAC SODIUM Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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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 Diclofenac Sodium (Diclofenac Sodium) which is also known as Diclofenac Sodium and Manufactured by NuCare Pharmaceuticals,Inc.. It is available in strength of 75 mg/1 per ml. Read more

Diclofenac Sodium (Diclofenac Sodium) 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

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • No data
  • Rx only
  • Cardiovascular Risk
  • Gastrointestinal Risk
  • ntttttttDiclofenac Sodium Delayed-release Tablets are a benzene-acetic acid derivative.tDiclofenac Sodium Delayed-release Tablets are available as delayed-release (delayed-release) tablets of 25 mg or 50 mg for oral administration. The chemical name is 2-[(2,6-dichlorophenyl)amino] benzeneacetic acid, monosodium salt. The molecular weight is 318.14. Its molecular formula is Cn n n Hn n n Cln n n NNaOn n n , and it has the following structural formulantttttttn nn
  • ntttttttThe inactive ingredients in Diclofenac Sodium Delayed-release Tablets include: lactose (monohydrate), microcrystalline cellulose, croscarmellose sodium, povidone, talc, magnesium stearate, methacrylic acid copolymer, polyethylene glycol, opadry brown (Titanium dioxide, hypromellose, polyethylene glycol, iron oxide red, iron oxide yellow)tand purified water.ntttttt
  • No data
  • Carefully consider the potential benefits and risks of Diclofenac Sodium Delayed-release Tablets and other treatment options before deciding to use Diclofenac Sodium Delayed-release Tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see n n n ).n nn
  • Diclofenac Sodium Delayed-release Tablets, are indicated:
  • Diclofenac Sodium Delayed-release Tablets are contraindicated in patients with known hypersensitivity to Diclofenac.
  • Diclofenac Sodium Delayed-release Tablets should not be given to patients who have experienced asthma, urticaria, or other allergic-type reactions after taking aspirin or other NSAIDs. Severe, rarely fatal, anaphylactic-like reactions to NSAIDs have been reported in such patients (see n n n n and n n n ).n nn
  • Diclofenac Sodium Delayed-release Tablets are contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery (see n n n ).n nn
  • No data
  • No data
  • In patients taking Diclofenac Sodium Delayed-release Tablets, or other NSAIDs, the most frequently reported adverse experiences occurring in approximately 1%-10% of patients are:
  • Gastrointestinal experiences including: abdominal pain, constipation, diarrhea, dyspepsia, flatulence, gross bleeding/perforation, heartburn, nausea, GI ulcers (gastric/duodenal) and vomiting.
  • Abnormal renal function, anemia, dizziness, edema, elevated liver enzymes, headaches, increased bleeding time, pruritus, rashes and tinnitus.
  • Additional adverse experiences reported occasionally include:
  • Arrayn- Body as a Whole:
  • Arrayn- Cardiovascular System:
  • Arrayn- Digestive System:
  • Arrayn- Hemic and Lymphatic System:
  • Arrayn- Metabolic and Nutritional:
  • Arrayn- Nervous System:
  • Arrayn- Respiratory System:
  • Arrayn- Skin and Appendages:
  • Arrayn- Special Senses:
  • Arrayn- Urogenital System:
  • Other adverse reactions, which occur rarely are:
  • Arrayn- Body as a Whole:
  • Arrayn- Cardiovascular System:
  • Arrayn- Digestive System:
  • Arrayn- Hemic and Lymphatic System:
  • Arrayn- Metabolic and Nutritional:
  • Arrayn- Nervous System:
  • Arrayn- Respiratory System:
  • Arrayn- Skin and Appendages:
  • Arrayn- Special Senses:
  • To report SUSPECTED ADVERSE REACTIONS, contact Unique Pharmaceutical Laboratories toll-free at (800) 521-5340 or FDA at 1-800-FDA-1088 or n- Array
  • Symptoms following acute NSAID overdoses are usually limited to lethargy, drowsiness, nausea, vomiting, and epigastric pain, which are generally reversible with supportive care. Gastrointestinal bleeding can occur. Hypertension, acute renal failure, respiratory depression and coma may occur, but are rare. Anaphylactoid reactions have been reported with therapeutic ingestion of NSAIDs, and may occur following an overdose.
  • Patients should be managed by symptomatic and supportive care following a NSAID overdose. There are no specific antidotes. Emesis and/or activated charcoal (60 to 100 g in adults, 1 to 2 g/kg in children) and/or osmotic cathartic may be indicated in patients seen within 4 hours of ingestion with symptoms or following a large overdose (5 to 10 times the usual dose). Forced diuresis, alkalinization of urine, hemodialysis, or hemoperfusion may not be useful due to high protein binding.
  • Carefully consider the potential benefits and risks of Diclofenac Sodium Delayed-release Tablets and other treatment options before deciding to use Diclofenac Sodium Delayed-release Tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see n ).n
  • After observing the response to initial therapy with Diclofenac Sodium Delayed-release Tablets, the dose and frequency should be adjusted to suit an individual patientu2019s needs.
  • For the relief of osteoarthritis, the recommended dosage is 100-150 mg/day in divided doses (50 mg b.i.d. or t.i.d., or 75 mg b.i.d.).
  • For the relief of rheumatoid arthritis, the recommended dosage is 150-200 mg/day in divided doses (50 mg t.i.d. or q.i.d., or 75 mg b.i.d.).
  • For the relief of ankylosing spondylitis, the recommended dosage is 100-125 mg/day, administered as 25 mg q.i.d., with an extra 25-mg dose at bedtime if necessary.
  • Different formulations of Diclofenac (Diclofenac sodium enteric-coated tablets; Diclofenac sodium extended-release tablets, Diclofenac potassium immediate-release tablets) are not necessarily bioequivalent even if the milligram strength is the same.
  • 75 mg
  • NDC 66267-071-14 Bottles of 14
  • Store at 20u00b0-25u00b0C (68u00b0-77u00b0F) (see USP Controlled Room Temperature). Protect from moisture.
  • Dispense in a tight, light-resistant container.
  • Manufactured by:n n n n n n(A Div. of J. B. Chemicals & Pharmaceuticals Ltd.)n n nMumbai 400 030, India.n
  • Distributed by:n n n n n nBuffalo Grove, IL 60089n
  • No data
  • No data

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