AcipHex - 63629-2733-2 - (rabeprazole sodium)

Alphabetical Index


Drug Information of AcipHex

Product NDC: 63629-2733
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of AcipHex

Product NDC: 63629-2733
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020973
Marketing Category: NDA
Start Marketing Date: 19990819

Package Information of AcipHex

Package NDC: 63629-2733-2
Package Description: 90 TABLET, COATED in 1 BOTTLE (63629-2733-2)

NDC Information of AcipHex

NDC Code 63629-2733-2
Proprietary Name AcipHex
Package Description 90 TABLET, COATED in 1 BOTTLE (63629-2733-2)
Product NDC 63629-2733
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rabeprazole sodium
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19990819
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
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