Omeprazole - 49999-265-90 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 49999-265
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole

Product NDC: 49999-265
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075576
Marketing Category: ANDA
Start Marketing Date: 20101013

Package Information of Omeprazole

Package NDC: 49999-265-90
Package Description: 90 CAPSULE in 1 BOTTLE (49999-265-90)

NDC Information of Omeprazole

NDC Code 49999-265-90
Proprietary Name Omeprazole
Package Description 90 CAPSULE in 1 BOTTLE (49999-265-90)
Product NDC 49999-265
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101013
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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