Ranitidine (Ranitidine)

Trade Name : Ranitidine

Teva Pharmaceuticals USA, Inc.

TABLET, FILM COATED

Strength 150 mg/1

RANITIDINE HYDROCHLORIDE Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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You can fill in a request for your medicine through the form provided. You can access the form by clicking on the ‘Get Price’ button.

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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 (Ranitidine) which is also known as Ranitidine and Manufactured by Teva Pharmaceuticals USA, Inc.. It is available in strength of 150 mg/1 per ml. Read more

Ranitidine (Ranitidine) 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 USP is a histamine H -receptor antagonist. Chemically it is N[2-[[[5- [(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-Nu00b4-methyl-2-nitro-1,1-ethenediamine, hydrochloride.
  • 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. The structural formula is:
  • C HNOSu2022HCl M.W. 350.87
  • Each tablet, for oral administration, contains 168 mg or 336 mg of ranitidine HCl equivalent to 150 mg or 300 mg of ranitidine, respectively. In addition, each tablet contains the following inactive ingredients: croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, red iron oxide, titanium dioxide, triethyl citrate and yellow iron oxide.
  • 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 an anticholinergic agent.
  • Ranitidine Tablets USP are 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 Tablets are contraindicated for 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 are available as beige, unscored, round, film-coated tablets debossed
  • 4357u201d on one side and u201c150u201d on the other side containing 150 mg ranitidine as ranitidine hydrochloride packaged in bottles of 60 and 500 tablets.
  • Ranitidine Tablets USP, 300 mg are available as beige, unscored, oval, film-coated tablets debossed
  • 4358u201d on one side and u201c300u201d on the other side containing 300 mg ranitidine as ranitidine hydrochloride packaged in bottles of 30, and 100 tablets.
  • PHARMACIST: Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).
  • Store at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F) in a dry place [See USP Controlled Room Temperature].
  • PROTECT FROM LIGHT
  • Replace cap securely after each opening.
  • Rev. B 10/2009
  • Manufactured In India By:
  • EMCURE PHARMACEUTICALS LTD.
  • Hinjwadi, Pune, India
  • Manufactured For:
  • TEVA PHARMACEUTICALS USA
  • Sellersville, PA 18960
  • RANITIDINE TABLETS USP
  • No data
  • No data

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