Acarbose - 16252-524-01 - (Acarbose)

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Drug Information of Acarbose

Product NDC: 16252-524
Proprietary Name: Acarbose
Non Proprietary Name: Acarbose
Active Ingredient(s): 50    mg/1 & nbsp;   Acarbose
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acarbose

Product NDC: 16252-524
Labeler Name: Cobalt Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077532
Marketing Category: ANDA
Start Marketing Date: 20080507

Package Information of Acarbose

Package NDC: 16252-524-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (16252-524-01)

NDC Information of Acarbose

NDC Code 16252-524-01
Proprietary Name Acarbose
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (16252-524-01)
Product NDC 16252-524
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acarbose
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080507
Marketing Category Name ANDA
Labeler Name Cobalt Laboratories
Substance Name ACARBOSE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]

Complete Information of Acarbose


General Information