Famotidine - 55315-035-31 - (Famotidine)

Alphabetical Index


Drug Information of Famotidine

Product NDC: 55315-035
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 55315-035
Labeler Name: Fred's Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090283
Marketing Category: ANDA
Start Marketing Date: 20100625

Package Information of Famotidine

Package NDC: 55315-035-31
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (55315-035-31)

NDC Information of Famotidine

NDC Code 55315-035-31
Proprietary Name Famotidine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (55315-035-31)
Product NDC 55315-035
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100625
Marketing Category Name ANDA
Labeler Name Fred's Inc.
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Famotidine


General Information