Omeprazole - 24236-656-24 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 24236-656
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: 24236-656
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075576
Marketing Category: ANDA
Start Marketing Date: 20130319

Package Information of Omeprazole

Package NDC: 24236-656-24
Package Description: 200 CAPSULE, DELAYED RELEASE in 1 CANISTER (24236-656-24)

NDC Information of Omeprazole

NDC Code 24236-656-24
Proprietary Name Omeprazole
Package Description 200 CAPSULE, DELAYED RELEASE in 1 CANISTER (24236-656-24)
Product NDC 24236-656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130319
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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