Aciphex - 54868-4185-2 - (rabeprazole sodium)

Alphabetical Index


Drug Information of Aciphex

Product NDC: 54868-4185
Proprietary Name: Aciphex
Non Proprietary Name: rabeprazole sodium
Active Ingredient(s): 20    mg/1 & nbsp;   rabeprazole sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Aciphex

Product NDC: 54868-4185
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020973
Marketing Category: NDA
Start Marketing Date: 20000515

Package Information of Aciphex

Package NDC: 54868-4185-2
Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (54868-4185-2)

NDC Information of Aciphex

NDC Code 54868-4185-2
Proprietary Name Aciphex
Package Description 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (54868-4185-2)
Product NDC 54868-4185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rabeprazole sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20000515
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name RABEPRAZOLE SODIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Aciphex


General Information