Glipizide - 52959-822-00 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 52959-822
Proprietary Name: Glipizide
Non Proprietary Name: Glipizide
Active Ingredient(s): 10    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 52959-822
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19950227

Package Information of Glipizide

Package NDC: 52959-822-00
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (52959-822-00)

NDC Information of Glipizide

NDC Code 52959-822-00
Proprietary Name Glipizide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (52959-822-00)
Product NDC 52959-822
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 H.J. Harkins Company, Inc.
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information