Home > National Drug Code (NDC) > Ranitidine Hydrochloride

Ranitidine Hydrochloride - 0781-1883-01 - (Ranitidine Hydrochloride)

Alphabetical Index


Drug Information of Ranitidine Hydrochloride

Product NDC: 0781-1883
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 150    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: 0781-1883
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: 0781-1883-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0781-1883-01)

NDC Information of Ranitidine Hydrochloride

NDC Code 0781-1883-01
Proprietary Name Ranitidine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0781-1883-01)
Product NDC 0781-1883
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 150
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine Hydrochloride


General Information