PEPCID - 0006-0963-31 - (famotidine)

Alphabetical Index


Drug Information of PEPCID

Product NDC: 0006-0963
Proprietary Name: PEPCID
Non Proprietary Name: famotidine
Active Ingredient(s): 20    mg/1 & nbsp;   famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of PEPCID

Product NDC: 0006-0963
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019462
Marketing Category: NDA
Start Marketing Date: 19861015

Package Information of PEPCID

Package NDC: 0006-0963-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0006-0963-31)

NDC Information of PEPCID

NDC Code 0006-0963-31
Proprietary Name PEPCID
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0006-0963-31)
Product NDC 0006-0963
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name famotidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19861015
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of PEPCID


General Information