Omeprazole - 51079-007-19 - (omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 51079-007
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: 51079-007
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075876
Marketing Category: ANDA
Start Marketing Date: 20121114

Package Information of Omeprazole

Package NDC: 51079-007-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-007-19) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (51079-007-17)

NDC Information of Omeprazole

NDC Code 51079-007-19
Proprietary Name Omeprazole
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-007-19) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (51079-007-17)
Product NDC 51079-007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20121114
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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