Glipizide - 55154-6224-9 - (glipizide)

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Drug Information of Glipizide

Product NDC: 55154-6224
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: 55154-6224
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074226
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Glipizide

Package NDC: 55154-6224-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6224-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Glipizide

NDC Code 55154-6224-9
Proprietary Name Glipizide
Package Description 6 BLISTER PACK in 1 CARTON (55154-6224-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-6224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110520
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information