Omeprazole - 33261-117-02 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 33261-117
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 10    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: 33261-117
Labeler Name: Aidarex Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075576
Marketing Category: ANDA
Start Marketing Date: 20090121

Package Information of Omeprazole

Package NDC: 33261-117-02
Package Description: 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-02)

NDC Information of Omeprazole

NDC Code 33261-117-02
Proprietary Name Omeprazole
Package Description 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-02)
Product NDC 33261-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20090121
Marketing Category Name ANDA
Labeler Name Aidarex Pharmaceuticals LLC
Substance Name OMEPRAZOLE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole


General Information