Glipizide - 0591-0460-10 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 0591-0460
Proprietary Name: Glipizide
Non Proprietary Name: Glipizide
Active Ingredient(s): 5    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 0591-0460
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19950227

Package Information of Glipizide

Package NDC: 0591-0460-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0591-0460-10)

NDC Information of Glipizide

NDC Code 0591-0460-10
Proprietary Name Glipizide
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0591-0460-10)
Product NDC 0591-0460
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950227
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name GLIPIZIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information