Glipizide - 54868-3319-7 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 54868-3319
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: 54868-3319
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19941118

Package Information of Glipizide

Package NDC: 54868-3319-7
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC (54868-3319-7)

NDC Information of Glipizide

NDC Code 54868-3319-7
Proprietary Name Glipizide
Package Description 180 TABLET in 1 BOTTLE, PLASTIC (54868-3319-7)
Product NDC 54868-3319
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19941118
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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