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AcetaZOLAMIDE - 0527-1050-10 - (Acetazolamide)

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Drug Information of AcetaZOLAMIDE

Product NDC: 0527-1050
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: 0527-1050
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084840
Marketing Category: ANDA
Start Marketing Date: 19780331

Package Information of AcetaZOLAMIDE

Package NDC: 0527-1050-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0527-1050-10)

NDC Information of AcetaZOLAMIDE

NDC Code 0527-1050-10
Proprietary Name AcetaZOLAMIDE
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0527-1050-10)
Product NDC 0527-1050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetazolamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19780331
Marketing Category Name ANDA
Labeler Name Lannett Company, 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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