FAMOTIDINE - 63629-2904-6 - (FAMOTIDINE)

Alphabetical Index


Drug Information of FAMOTIDINE

Product NDC: 63629-2904
Proprietary Name: FAMOTIDINE
Non Proprietary Name: FAMOTIDINE
Active Ingredient(s): 20    mg/1 & nbsp;   FAMOTIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FAMOTIDINE

Product NDC: 63629-2904
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090837
Marketing Category: ANDA
Start Marketing Date: 20100806

Package Information of FAMOTIDINE

Package NDC: 63629-2904-6
Package Description: 10 TABLET in 1 BOTTLE (63629-2904-6)

NDC Information of FAMOTIDINE

NDC Code 63629-2904-6
Proprietary Name FAMOTIDINE
Package Description 10 TABLET in 1 BOTTLE (63629-2904-6)
Product NDC 63629-2904
Product Type Name HUMAN OTC DRUG
Non Proprietary Name FAMOTIDINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100806
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of FAMOTIDINE


General Information