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Acetazolamide - 55289-221-24 - (Acetazolamide)

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Drug Information of Acetazolamide

Product NDC: 55289-221
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: 55289-221
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040195
Marketing Category: ANDA
Start Marketing Date: 19970528

Package Information of Acetazolamide

Package NDC: 55289-221-24
Package Description: 24 TABLET in 1 BOTTLE, PLASTIC (55289-221-24)

NDC Information of Acetazolamide

NDC Code 55289-221-24
Proprietary Name Acetazolamide
Package Description 24 TABLET in 1 BOTTLE, PLASTIC (55289-221-24)
Product NDC 55289-221
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 PD-Rx Pharmaceuticals, 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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