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Methazolamide - 0781-1072-01 - (Methazolamide)

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Drug Information of Methazolamide

Product NDC: 0781-1072
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: 0781-1072
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040036
Marketing Category: ANDA
Start Marketing Date: 19930630

Package Information of Methazolamide

Package NDC: 0781-1072-01
Package Description: 100 TABLET in 1 BOTTLE (0781-1072-01)

NDC Information of Methazolamide

NDC Code 0781-1072-01
Proprietary Name Methazolamide
Package Description 100 TABLET in 1 BOTTLE (0781-1072-01)
Product NDC 0781-1072
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methazolamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930630
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name METHAZOLAMIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Methazolamide


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