Glipizide - 0781-1452-13 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 0781-1452
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: 0781-1452
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074305
Marketing Category: ANDA
Start Marketing Date: 19950407

Package Information of Glipizide

Package NDC: 0781-1452-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-1452-13) > 10 TABLET in 1 BLISTER PACK

NDC Information of Glipizide

NDC Code 0781-1452-13
Proprietary Name Glipizide
Package Description 10 BLISTER PACK in 1 CARTON (0781-1452-13) > 10 TABLET in 1 BLISTER PACK
Product NDC 0781-1452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950407
Marketing Category Name ANDA
Labeler Name Sandoz 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