Omeprazole - 63739-445-10 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 63739-445
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: 63739-445
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075410
Marketing Category: ANDA
Start Marketing Date: 20091008

Package Information of Omeprazole

Package NDC: 63739-445-10
Package Description: 20 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-445-10) > 5 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK

NDC Information of Omeprazole

NDC Code 63739-445-10
Proprietary Name Omeprazole
Package Description 20 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-445-10) > 5 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK
Product NDC 63739-445
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 20091008
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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