NEXIUM - 21695-091-30 - (Esomeprazole magnesium)

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Drug Information of NEXIUM

Product NDC: 21695-091
Proprietary Name: NEXIUM
Non Proprietary Name: Esomeprazole magnesium
Active Ingredient(s): 20    mg/1 & nbsp;   Esomeprazole magnesium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of NEXIUM

Product NDC: 21695-091
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021153
Marketing Category: NDA
Start Marketing Date: 20110708

Package Information of NEXIUM

Package NDC: 21695-091-30
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (21695-091-30)

NDC Information of NEXIUM

NDC Code 21695-091-30
Proprietary Name NEXIUM
Package Description 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (21695-091-30)
Product NDC 21695-091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Esomeprazole magnesium
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110708
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name ESOMEPRAZOLE MAGNESIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of NEXIUM


General Information