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Methazolamide - 48102-100-01 - (methazolamide)

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Drug Information of Methazolamide

Product NDC: 48102-100
Proprietary Name: Methazolamide
Non Proprietary Name: methazolamide
Active Ingredient(s): 25    mg/1 & nbsp;   methazolamide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methazolamide

Product NDC: 48102-100
Labeler Name: Fera Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040062
Marketing Category: ANDA
Start Marketing Date: 20100622

Package Information of Methazolamide

Package NDC: 48102-100-01
Package Description: 100 TABLET in 1 BOTTLE (48102-100-01)

NDC Information of Methazolamide

NDC Code 48102-100-01
Proprietary Name Methazolamide
Package Description 100 TABLET in 1 BOTTLE (48102-100-01)
Product NDC 48102-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methazolamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100622
Marketing Category Name ANDA
Labeler Name Fera Pharmaceuticals
Substance Name METHAZOLAMIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Methazolamide


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