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Acetazolamide - 51672-4023-1 - (Acetazolamide)

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Drug Information of Acetazolamide

Product NDC: 51672-4023
Proprietary Name: Acetazolamide
Non Proprietary Name: Acetazolamide
Active Ingredient(s): 250    mg/1 & nbsp;   Acetazolamide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetazolamide

Product NDC: 51672-4023
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040195
Marketing Category: ANDA
Start Marketing Date: 19970528

Package Information of Acetazolamide

Package NDC: 51672-4023-1
Package Description: 100 TABLET in 1 BOTTLE (51672-4023-1)

NDC Information of Acetazolamide

NDC Code 51672-4023-1
Proprietary Name Acetazolamide
Package Description 100 TABLET in 1 BOTTLE (51672-4023-1)
Product NDC 51672-4023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetazolamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970528
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name ACETAZOLAMIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [Chemical/Ingredient]

Complete Information of Acetazolamide


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