Glipizide - 0591-0900-01 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 0591-0900
Proprietary Name: Glipizide
Non Proprietary Name: Glipizide
Active Ingredient(s): 2.5    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 0591-0900
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076467
Marketing Category: ANDA
Start Marketing Date: 20060401

Package Information of Glipizide

Package NDC: 0591-0900-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-0900-01)

NDC Information of Glipizide

NDC Code 0591-0900-01
Proprietary Name Glipizide
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-0900-01)
Product NDC 0591-0900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060401
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
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