omeprazole - 41250-915-02 - (Omeprazole)

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Drug Information of omeprazole

Product NDC: 41250-915
Proprietary Name: omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of omeprazole

Product NDC: 41250-915
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080229

Package Information of omeprazole

Package NDC: 41250-915-02
Package Description: 2 BOTTLE in 1 CARTON (41250-915-02) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE

NDC Information of omeprazole

NDC Code 41250-915-02
Proprietary Name omeprazole
Package Description 2 BOTTLE in 1 CARTON (41250-915-02) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC 41250-915
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080229
Marketing Category Name NDA
Labeler Name Meijer Distribution Inc
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of omeprazole


General Information