Prevacid - 64764-541-05 - (lansoprazole)

Alphabetical Index


Drug Information of Prevacid

Product NDC: 64764-541
Proprietary Name: Prevacid
Non Proprietary Name: lansoprazole
Active Ingredient(s): 15    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: 64764-541
Labeler Name: Takeda Pharmaceuticals America, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020406
Marketing Category: NDA
Start Marketing Date: 19950510

Package Information of Prevacid

Package NDC: 64764-541-05
Package Description: 5 BLISTER PACK in 1 TRAY (64764-541-05) > 4 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Prevacid

NDC Code 64764-541-05
Proprietary Name Prevacid
Package Description 5 BLISTER PACK in 1 TRAY (64764-541-05) > 4 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 64764-541
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 Takeda Pharmaceuticals America, Inc.
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Prevacid


General Information