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Ranitidine Hydrochloride - 63629-1672-8 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 63629-1672
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: 63629-1672
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074467
Marketing Category: ANDA
Start Marketing Date: 19970829

Package Information of Ranitidine Hydrochloride

Package NDC: 63629-1672-8
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (63629-1672-8)

NDC Information of Ranitidine Hydrochloride

NDC Code 63629-1672-8
Proprietary Name Ranitidine Hydrochloride
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (63629-1672-8)
Product NDC 63629-1672
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 Bryant Ranch Prepack
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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