FAMOTIDINE - 64679-972-02 - (FAMOTIDINE)

Alphabetical Index


Drug Information of FAMOTIDINE

Product NDC: 64679-972
Proprietary Name: FAMOTIDINE
Non Proprietary Name: FAMOTIDINE
Active Ingredient(s): 10    mg/1 & nbsp;   FAMOTIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FAMOTIDINE

Product NDC: 64679-972
Labeler Name: WOCKHARDT USA LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077146
Marketing Category: ANDA
Start Marketing Date: 20050307

Package Information of FAMOTIDINE

Package NDC: 64679-972-02
Package Description: 10 BLISTER PACK in 1 CARTON (64679-972-02) > 10 TABLET in 1 BLISTER PACK

NDC Information of FAMOTIDINE

NDC Code 64679-972-02
Proprietary Name FAMOTIDINE
Package Description 10 BLISTER PACK in 1 CARTON (64679-972-02) > 10 TABLET in 1 BLISTER PACK
Product NDC 64679-972
Product Type Name HUMAN OTC DRUG
Non Proprietary Name FAMOTIDINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050307
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC.
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of FAMOTIDINE


General Information