Glipizide - 55154-0534-4 - (glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 55154-0534
Proprietary Name: Glipizide
Non Proprietary Name: glipizide
Active Ingredient(s): 2.5    mg/1 & nbsp;   glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 55154-0534
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020329
Marketing Category: NDA
Start Marketing Date: 19940426

Package Information of Glipizide

Package NDC: 55154-0534-4
Package Description: 30 POUCH in 1 CARTON (55154-0534-4) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (55154-0534-6)

NDC Information of Glipizide

NDC Code 55154-0534-4
Proprietary Name Glipizide
Package Description 30 POUCH in 1 CARTON (55154-0534-4) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (55154-0534-6)
Product NDC 55154-0534
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glipizide
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19940426
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name GLIPIZIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information