Omeprazole - 0179-0016-70 - (Omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 0179-0016
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 40    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole

Product NDC: 0179-0016
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075347
Marketing Category: ANDA
Start Marketing Date: 20090801

Package Information of Omeprazole

Package NDC: 0179-0016-70
Package Description: 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOX, UNIT-DOSE (0179-0016-70)

NDC Information of Omeprazole

NDC Code 0179-0016-70
Proprietary Name Omeprazole
Package Description 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOX, UNIT-DOSE (0179-0016-70)
Product NDC 0179-0016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 20090801
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name OMEPRAZOLE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole


General Information