PRILOSEC - 0186-0625-01 - (Omeprazole magnesium)

Alphabetical Index


Drug Information of PRILOSEC

Product NDC: 0186-0625
Proprietary Name: PRILOSEC
Non Proprietary Name: Omeprazole magnesium
Active Ingredient(s): 2.5    mg/1 & nbsp;   Omeprazole magnesium
Administration Route(s): ORAL
Dosage Form(s): GRANULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PRILOSEC

Product NDC: 0186-0625
Labeler Name: AstraZeneca LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022056
Marketing Category: NDA
Start Marketing Date: 20020209

Package Information of PRILOSEC

Package NDC: 0186-0625-01
Package Description: 30 GRANULE, DELAYED RELEASE in 1 CARTON (0186-0625-01)

NDC Information of PRILOSEC

NDC Code 0186-0625-01
Proprietary Name PRILOSEC
Package Description 30 GRANULE, DELAYED RELEASE in 1 CARTON (0186-0625-01)
Product NDC 0186-0625
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole magnesium
Dosage Form Name GRANULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20020209
Marketing Category Name NDA
Labeler Name AstraZeneca LP
Substance Name OMEPRAZOLE MAGNESIUM
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of PRILOSEC


General Information