PRILOSEC - 0186-0742-82 - (Omeprazole magnesium)

Alphabetical Index


Drug Information of PRILOSEC

Product NDC: 0186-0742
Proprietary Name: PRILOSEC
Non Proprietary Name: Omeprazole magnesium
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole magnesium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PRILOSEC

Product NDC: 0186-0742
Labeler Name: AstraZeneca LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019810
Marketing Category: NDA
Start Marketing Date: 19901001

Package Information of PRILOSEC

Package NDC: 0186-0742-82
Package Description: 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-0742-82)

NDC Information of PRILOSEC

NDC Code 0186-0742-82
Proprietary Name PRILOSEC
Package Description 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-0742-82)
Product NDC 0186-0742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole magnesium
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19901001
Marketing Category Name NDA
Labeler Name AstraZeneca LP
Substance Name OMEPRAZOLE MAGNESIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of PRILOSEC


General Information