Home > National Drug Code (NDC) > acid reducer

acid reducer - 41250-950-02 - (Ranitidine)

Alphabetical Index


Drug Information of acid reducer

Product NDC: 41250-950
Proprietary Name: acid reducer
Non Proprietary Name: Ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of acid reducer

Product NDC: 41250-950
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091429
Marketing Category: ANDA
Start Marketing Date: 20110921

Package Information of acid reducer

Package NDC: 41250-950-02
Package Description: 1 BOTTLE in 1 CARTON (41250-950-02) > 24 TABLET, FILM COATED in 1 BOTTLE

NDC Information of acid reducer

NDC Code 41250-950-02
Proprietary Name acid reducer
Package Description 1 BOTTLE in 1 CARTON (41250-950-02) > 24 TABLET, FILM COATED in 1 BOTTLE
Product NDC 41250-950
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110921
Marketing Category Name ANDA
Labeler Name Meijer Distribution Inc
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acid reducer


General Information