AcipHex - 49999-447-30 - (rabeprazole sodium)

Alphabetical Index


Drug Information of AcipHex

Product NDC: 49999-447
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: 49999-447
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Produtcs LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020973
Marketing Category: NDA
Start Marketing Date: 20120217

Package Information of AcipHex

Package NDC: 49999-447-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (49999-447-30)

NDC Information of AcipHex

NDC Code 49999-447-30
Proprietary Name AcipHex
Package Description 30 TABLET, COATED in 1 BOTTLE (49999-447-30)
Product NDC 49999-447
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rabeprazole sodium
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120217
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Produtcs LLC
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