omeprazole - 11822-0915-1 - (Omeprazole)

Alphabetical Index


Drug Information of omeprazole

Product NDC: 11822-0915
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: 11822-0915
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080225

Package Information of omeprazole

Package NDC: 11822-0915-1
Package Description: 2 CARTON in 1 CARTON (11822-0915-1) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of omeprazole

NDC Code 11822-0915-1
Proprietary Name omeprazole
Package Description 2 CARTON in 1 CARTON (11822-0915-1) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 11822-0915
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080225
Marketing Category Name NDA
Labeler Name Rite Aid Corporation
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of omeprazole


General Information