Omeprazole - 52959-722-15 - (Omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 52959-722
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole

Product NDC: 52959-722
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075876
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Omeprazole

Package NDC: 52959-722-15
Package Description: 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (52959-722-15)

NDC Information of Omeprazole

NDC Code 52959-722-15
Proprietary Name Omeprazole
Package Description 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (52959-722-15)
Product NDC 52959-722
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110114
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole


General Information