omeprazole - 37808-915-55 - (Omeprazole)

Alphabetical Index


Drug Information of omeprazole

Product NDC: 37808-915
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: 37808-915
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080229

Package Information of omeprazole

Package NDC: 37808-915-55
Package Description: 3 CARTON in 1 CARTON (37808-915-55) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of omeprazole

NDC Code 37808-915-55
Proprietary Name omeprazole
Package Description 3 CARTON in 1 CARTON (37808-915-55) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 37808-915
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 H E B
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of omeprazole


General Information