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Ranitidine Hydrochloride - 0781-1884-13 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 0781-1884
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine Hydrochloride

Product NDC: 0781-1884
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074467
Marketing Category: ANDA
Start Marketing Date: 19970829

Package Information of Ranitidine Hydrochloride

Package NDC: 0781-1884-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-1884-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ranitidine Hydrochloride

NDC Code 0781-1884-13
Proprietary Name Ranitidine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (0781-1884-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0781-1884
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970829
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine Hydrochloride


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