Acarbose - 54868-5945-0 - (Acarbose)

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Drug Information of Acarbose

Product NDC: 54868-5945
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: 54868-5945
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078470
Marketing Category: ANDA
Start Marketing Date: 20081003

Package Information of Acarbose

Package NDC: 54868-5945-0
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-5945-0)

NDC Information of Acarbose

NDC Code 54868-5945-0
Proprietary Name Acarbose
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-5945-0)
Product NDC 54868-5945
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acarbose
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081003
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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