Pepcid AC - 16837-872-21 - (Famotidine)

Alphabetical Index


Drug Information of Pepcid AC

Product NDC: 16837-872
Proprietary Name: Pepcid AC
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 Pepcid AC

Product NDC: 16837-872
Labeler Name: McNeil Consumer Pharmaceuticals Co.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020325
Marketing Category: NDA
Start Marketing Date: 19951001

Package Information of Pepcid AC

Package NDC: 16837-872-21
Package Description: 4 BLISTER PACK in 1 CARTON (16837-872-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Pepcid AC

NDC Code 16837-872-21
Proprietary Name Pepcid AC
Package Description 4 BLISTER PACK in 1 CARTON (16837-872-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 16837-872
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19951001
Marketing Category Name NDA
Labeler Name McNeil Consumer Pharmaceuticals Co.
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pepcid AC


General Information