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Acetazolamide - 25021-817-10 - (acetazolamide sodium)

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Drug Information of Acetazolamide

Product NDC: 25021-817
Proprietary Name: Acetazolamide
Non Proprietary Name: acetazolamide sodium
Active Ingredient(s): 500    mg/5mL & nbsp;   acetazolamide sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Acetazolamide

Product NDC: 25021-817
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200880
Marketing Category: ANDA
Start Marketing Date: 20120615

Package Information of Acetazolamide

Package NDC: 25021-817-10
Package Description: 1 VIAL in 1 CARTON (25021-817-10) > 5 mL in 1 VIAL

NDC Information of Acetazolamide

NDC Code 25021-817-10
Proprietary Name Acetazolamide
Package Description 1 VIAL in 1 CARTON (25021-817-10) > 5 mL in 1 VIAL
Product NDC 25021-817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetazolamide sodium
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120615
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name ACETAZOLAMIDE SODIUM
Strength Number 500
Strength Unit mg/5mL
Pharmaceutical Classes Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [Chemical/Ingredient]

Complete Information of Acetazolamide


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