Acarbose - 23155-147-05 - (Acarbose)

Alphabetical Index


Drug Information of Acarbose

Product NDC: 23155-147
Proprietary Name: Acarbose
Non Proprietary Name: Acarbose
Active Ingredient(s): 25    mg/1 & nbsp;   Acarbose
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acarbose

Product NDC: 23155-147
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202271
Marketing Category: ANDA
Start Marketing Date: 20120730

Package Information of Acarbose

Package NDC: 23155-147-05
Package Description: 500 TABLET in 1 BOTTLE (23155-147-05)

NDC Information of Acarbose

NDC Code 23155-147-05
Proprietary Name Acarbose
Package Description 500 TABLET in 1 BOTTLE (23155-147-05)
Product NDC 23155-147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acarbose
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120730
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name ACARBOSE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]

Complete Information of Acarbose


General Information