Omeprazole - 55154-3326-0 - (Omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 55154-3326
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: 55154-3326
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075757
Marketing Category: ANDA
Start Marketing Date: 20100504

Package Information of Omeprazole

Package NDC: 55154-3326-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3326-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Omeprazole

NDC Code 55154-3326-0
Proprietary Name Omeprazole
Package Description 10 BLISTER PACK in 1 BAG (55154-3326-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55154-3326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100504
Marketing Category Name ANDA
Labeler Name Cardinal Health
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