Glipizide - 54868-3318-3 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 54868-3318
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: 54868-3318
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19940726

Package Information of Glipizide

Package NDC: 54868-3318-3
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-3318-3)

NDC Information of Glipizide

NDC Code 54868-3318-3
Proprietary Name Glipizide
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-3318-3)
Product NDC 54868-3318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19940726
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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