Omeprazole - 54868-5911-0 - (omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 54868-5911
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: 54868-5911
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080619

Package Information of Omeprazole

Package NDC: 54868-5911-0
Package Description: 6 BLISTER PACK in 1 CARTON (54868-5911-0) > 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Omeprazole

NDC Code 54868-5911-0
Proprietary Name Omeprazole
Package Description 6 BLISTER PACK in 1 CARTON (54868-5911-0) > 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 54868-5911
Product Type Name HUMAN OTC DRUG
Non Proprietary Name omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080619
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Omeprazole


General Information