Prevacid - 55289-704-07 - (lansoprazole)

Alphabetical Index


Drug Information of Prevacid

Product NDC: 55289-704
Proprietary Name: Prevacid
Non Proprietary Name: lansoprazole
Active Ingredient(s): 30    mg/1 & nbsp;   lansoprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Prevacid

Product NDC: 55289-704
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020406
Marketing Category: NDA
Start Marketing Date: 19950510

Package Information of Prevacid

Package NDC: 55289-704-07
Package Description: 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55289-704-07)

NDC Information of Prevacid

NDC Code 55289-704-07
Proprietary Name Prevacid
Package Description 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55289-704-07)
Product NDC 55289-704
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19950510
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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