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Acetazolamide - 23155-120-01 - (Acetazolamide)

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Drug Information of Acetazolamide

Product NDC: 23155-120
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: 23155-120
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090779
Marketing Category: ANDA
Start Marketing Date: 20120924

Package Information of Acetazolamide

Package NDC: 23155-120-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (23155-120-01)

NDC Information of Acetazolamide

NDC Code 23155-120-01
Proprietary Name Acetazolamide
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (23155-120-01)
Product NDC 23155-120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetazolamide
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120924
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
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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