Famotidine - 55111-396-16 - (Famotidine)

Alphabetical Index


Drug Information of Famotidine

Product NDC: 55111-396
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: 55111-396
Labeler Name: Dr.Reddys Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077367
Marketing Category: ANDA
Start Marketing Date: 20060930

Package Information of Famotidine

Package NDC: 55111-396-16
Package Description: 5 BLISTER PACK in 1 CARTON (55111-396-16) > 5 TABLET in 1 BLISTER PACK

NDC Information of Famotidine

NDC Code 55111-396-16
Proprietary Name Famotidine
Package Description 5 BLISTER PACK in 1 CARTON (55111-396-16) > 5 TABLET in 1 BLISTER PACK
Product NDC 55111-396
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060930
Marketing Category Name ANDA
Labeler Name Dr.Reddys Laboratories Limited
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Famotidine


General Information