Home > National Drug Code (NDC) > acid reducer

acid reducer - 41250-141-72 - (Famotidine)

Alphabetical Index


Drug Information of acid reducer

Product NDC: 41250-141
Proprietary Name: acid reducer
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 acid reducer

Product NDC: 41250-141
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075400
Marketing Category: ANDA
Start Marketing Date: 20091014

Package Information of acid reducer

Package NDC: 41250-141-72
Package Description: 1 BOTTLE in 1 CARTON (41250-141-72) > 60 TABLET in 1 BOTTLE

NDC Information of acid reducer

NDC Code 41250-141-72
Proprietary Name acid reducer
Package Description 1 BOTTLE in 1 CARTON (41250-141-72) > 60 TABLET in 1 BOTTLE
Product NDC 41250-141
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091014
Marketing Category Name ANDA
Labeler Name Meijer Distribution Inc
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acid reducer


General Information