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Ranitidine Hydrochloride (Ranitidine Hydrochloride)

Trade Name : Ranitidine Hydrochloride

Sandoz Inc

TABLET, FILM COATED

Strength 150 mg/1

RANITIDINE HYDROCHLORIDE Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [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 Ranitidine Hydrochloride (Ranitidine Hydrochloride) which is also known as Ranitidine Hydrochloride and Manufactured by Sandoz Inc. It is available in strength of 150 mg/1 per ml. Read more

Ranitidine Hydrochloride (Ranitidine Hydrochloride) 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
  • Ranitidine hydrochloride (HCl), is a histamine H-receptor antagonist. Chemically it is -[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]--methyl-2-nitro-1,1-ethenediamine, HCl.
  • It has the following structure:
  • The empirical formula is CHNOS u2022 HCl, representing a molecular weight of 350.87.
  • Ranitidine HCl is a white to pale yellow, granular substance that is soluble in water. It has a slightly bitter taste and sulfur like odor.
  • Each tablet, for oral administration contains 167 mg or 335 mg of ranitidine hydrochloride USP equivalent to 150 mg and 300 mg of ranitidine, respectively. Inactive ingredients: D & C Red #30 Aluminum Lake, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, triethyl citrate, sodium starch glycolate, titanium dioxide, propylene glycol and flavoring. The also contains: D & C Yellow #10 Aluminum Lake.
  • Each capsule, for oral administration contains 167 mg or 335 mg of ranitidine hydrochloride USP equivalent to 150 mg and 300 mg of ranitidine, respectively. Inactive ingredients: Ammonium hydroxide, colloidal silicon dioxide, corn starch, FD & C Blue #1, FD & C Red #40, FD & C Yellow #6, gelatin, magnesium stearate, pharmaceutical glaze, propylene glycol, simethicone, sodium lauryl sulfate, sodium starch glycolate, and titanium dioxide.
  • Ranitidine is a competitive, reversible inhibitor of the action of histamine at the histamine H-receptors, including receptors on the gastric cells. Ranitidine does not lower serum Ca++ in hypercalcemic states. Ranitidine is not a anticholinergic agent.
  • Ranitidine is indicated in:
  • Concomitant antacids should be given as needed for pain relief to patients with active duodenal ulcer; active, benign gastric ulcer; hypersecretory states; GERD; and erosive esophagitis.
  • Ranitidine is contraindicated in patients known to have hypersensitivity to the drug or any of the ingredients (see ).
  • No data
  • The following have been reported as events in clinical trials or in the routine management of patients treated with ranitidine. The relationship to therapy with ranitidine has been unclear in many cases. Headache, sometimes severe, seems to be related to administration of ranitidine.
  • There has been limited experience with overdosage. Reported acute ingestions of up to 18 g orally have been associated with transient adverse effects similar to those encountered in normal clinical experience (see ). In addition, abnormalities of gait and hypotension have been reported.
  • When overdosage occurs, the usual measures to remove unabsorbed material from the gastrointestinal tract, clinical monitoring, and supportive therapy should be employed.
  • Studies in dogs receiving dosages of ranitidine in excess of 225 mg/kg per day have shown muscular tremors, vomiting, and rapid respiration. Single oral doses of 1,000 mg/kg in mice and rats were not lethal. Intravenous LD values in mice and rats were 77 and 83 mg/kg, respectively.
  • No data
  • Ranitidine Tablets, USP
  • 150 mg:
  • NDC 0781-1883-60 bottles of 60 tablets
  • NDC 0781-1883-01 bottles of 100 tablets
  • NDC 0781-1883-05 bottles of 500 tablets
  • NDC 0781-1883-10 bottles of 1000 tablets
  • 300 mg:
  • NDC 0781-1884-31 bottles of 30 tablets
  • NDC 0781-1884-25 bottles of 250 tablets
  • NDC 0781-1884-10 bottles of 1000 tablets
  • Ranitidine Capsules,
  • 150 mg:
  • NDC 0781-2855-31 bottles of 30 capsules
  • NDC 0781-2855-60 bottles of 60 capsules
  • NDC 0781-2855-92 bottles of 90 capsules
  • NDC 0781-2855-05 bottles of 500 capsules
  • 300 mg:
  • NDC 0781-2865-31 bottles of 30 capsules
  • NDC 0781-2865-92 bottles of 90 capsules
  • NDC 0781-2865-05 bottles of 500 capsules
  • Store at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F) [see USP Controlled Room Temperature] in a dry place. Protect from light. Replace cap securely after each opening.
  • Dispense in a tight, light-resistant container.
  • Manufactured by
  • Sandoz Inc.
  • Princeton, NJ 08540
  • Rev. December 2018
  • 7292
  • NDC 0781-1883-60
  • Ranitidine
  • Tablets, USP
  • 150 mg
  • Rx only
  • 60 Tablets
  • SANDOZ
  • NDC 0781-1884-31
  • Ranitidine
  • Tablets, USP
  • 300 mg
  • Rx only
  • 30 Tablets
  • SANDOZ
  • NDC 0781-2855-05
  • Ranitidine
  • Capsules
  • 150 mg
  • Rx only
  • 500 Capsules
  • SANDOZ
  • NDC 0781-2865-31
  • Ranitidine
  • Capsules
  • 300 mg
  • Rx only
  • 30 Capsules
  • SANDOZ

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