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Acetazolamide - 54569-4387-1 - (Acetazolamide)

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Drug Information of Acetazolamide

Product NDC: 54569-4387
Proprietary Name: Acetazolamide
Non Proprietary Name: Acetazolamide
Active Ingredient(s): 125    mg/1 & nbsp;   Acetazolamide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetazolamide

Product NDC: 54569-4387
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040195
Marketing Category: ANDA
Start Marketing Date: 19970528

Package Information of Acetazolamide

Package NDC: 54569-4387-1
Package Description: 12 TABLET in 1 BOTTLE (54569-4387-1)

NDC Information of Acetazolamide

NDC Code 54569-4387-1
Proprietary Name Acetazolamide
Package Description 12 TABLET in 1 BOTTLE (54569-4387-1)
Product NDC 54569-4387
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 A-S Medication Solutions LLC
Substance Name ACETAZOLAMIDE
Strength Number 125
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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