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Acetazolamide - 0179-0050-70 - (Acetazolamide)

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Drug Information of Acetazolamide

Product NDC: 0179-0050
Proprietary Name: Acetazolamide
Non Proprietary Name: Acetazolamide
Active Ingredient(s): 500    mg/1 & nbsp;   Acetazolamide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Acetazolamide

Product NDC: 0179-0050
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040904
Marketing Category: ANDA
Start Marketing Date: 20100209

Package Information of Acetazolamide

Package NDC: 0179-0050-70
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0179-0050-70)

NDC Information of Acetazolamide

NDC Code 0179-0050-70
Proprietary Name Acetazolamide
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0179-0050-70)
Product NDC 0179-0050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetazolamide
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100209
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name ACETAZOLAMIDE
Strength Number 500
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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