Glipizide - 21695-470-78 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 21695-470
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: 21695-470
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19950227

Package Information of Glipizide

Package NDC: 21695-470-78
Package Description: 180 TABLET in 1 BOTTLE (21695-470-78)

NDC Information of Glipizide

NDC Code 21695-470-78
Proprietary Name Glipizide
Package Description 180 TABLET in 1 BOTTLE (21695-470-78)
Product NDC 21695-470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950227
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information