Prevacid - 55154-0253-0 - (lansoprazole)

Alphabetical Index


Drug Information of Prevacid

Product NDC: 55154-0253
Proprietary Name: Prevacid
Non Proprietary Name: lansoprazole
Active Ingredient(s): 30    mg/1 & nbsp;   lansoprazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Prevacid

Product NDC: 55154-0253
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021428
Marketing Category: NDA
Start Marketing Date: 20020830

Package Information of Prevacid

Package NDC: 55154-0253-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0253-0) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Prevacid

NDC Code 55154-0253-0
Proprietary Name Prevacid
Package Description 10 BLISTER PACK in 1 BAG (55154-0253-0) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55154-0253
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20020830
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name LANSOPRAZOLE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Prevacid


General Information