Famotidine - 52959-116-60 - (Famotidine)

Alphabetical Index


Drug Information of Famotidine

Product NDC: 52959-116
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 40    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 52959-116
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075805
Marketing Category: ANDA
Start Marketing Date: 20010416

Package Information of Famotidine

Package NDC: 52959-116-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (52959-116-60)

NDC Information of Famotidine

NDC Code 52959-116-60
Proprietary Name Famotidine
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (52959-116-60)
Product NDC 52959-116
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010416
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name FAMOTIDINE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Famotidine


General Information