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Acetazolamide - 68382-261-10 - (Acetazolamide)

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Drug Information of Acetazolamide

Product NDC: 68382-261
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: 68382-261
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040904
Marketing Category: ANDA
Start Marketing Date: 20081215

Package Information of Acetazolamide

Package NDC: 68382-261-10
Package Description: 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-261-10)

NDC Information of Acetazolamide

NDC Code 68382-261-10
Proprietary Name Acetazolamide
Package Description 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-261-10)
Product NDC 68382-261
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetazolamide
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20081215
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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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