Omeprazole - 45865-342-15 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 45865-342
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: 45865-342
Labeler Name: Medsource Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075576
Marketing Category: ANDA
Start Marketing Date: 20081217

Package Information of Omeprazole

Package NDC: 45865-342-15
Package Description: 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (45865-342-15)

NDC Information of Omeprazole

NDC Code 45865-342-15
Proprietary Name Omeprazole
Package Description 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (45865-342-15)
Product NDC 45865-342
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20081217
Marketing Category Name ANDA
Labeler Name Medsource Pharmaceuticals
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