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AcetaZOLAMIDE - 68084-541-01 - (Acetazolamide)

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Drug Information of AcetaZOLAMIDE

Product NDC: 68084-541
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: 68084-541
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084840
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of AcetaZOLAMIDE

Package NDC: 68084-541-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-541-01) > 10 TABLET in 1 BLISTER PACK (68084-541-11)

NDC Information of AcetaZOLAMIDE

NDC Code 68084-541-01
Proprietary Name AcetaZOLAMIDE
Package Description 10 BLISTER PACK in 1 CARTON (68084-541-01) > 10 TABLET in 1 BLISTER PACK (68084-541-11)
Product NDC 68084-541
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetazolamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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