Glipizide - 21695-967-30 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 21695-967
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: 21695-967
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076467
Marketing Category: ANDA
Start Marketing Date: 20060401

Package Information of Glipizide

Package NDC: 21695-967-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-967-30)

NDC Information of Glipizide

NDC Code 21695-967-30
Proprietary Name Glipizide
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-967-30)
Product NDC 21695-967
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 Rebel Distributors Corp
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