FAMOTIDINE - 55648-374-07 - (FAMOTIDINE)

Alphabetical Index


Drug Information of FAMOTIDINE

Product NDC: 55648-374
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: 55648-374
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090837
Marketing Category: ANDA
Start Marketing Date: 20100806

Package Information of FAMOTIDINE

Package NDC: 55648-374-07
Package Description: 10 BLISTER PACK in 1 CARTON (55648-374-07) > 10 TABLET in 1 BLISTER PACK

NDC Information of FAMOTIDINE

NDC Code 55648-374-07
Proprietary Name FAMOTIDINE
Package Description 10 BLISTER PACK in 1 CARTON (55648-374-07) > 10 TABLET in 1 BLISTER PACK
Product NDC 55648-374
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 WOCKHARDT LIMITED
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of FAMOTIDINE


General Information