Glipizide - 51079-811-19 - (glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 51079-811
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: 51079-811
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074226
Marketing Category: ANDA
Start Marketing Date: 20101104

Package Information of Glipizide

Package NDC: 51079-811-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-811-19) > 1 TABLET in 1 BLISTER PACK (51079-811-17)

NDC Information of Glipizide

NDC Code 51079-811-19
Proprietary Name Glipizide
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-811-19) > 1 TABLET in 1 BLISTER PACK (51079-811-17)
Product NDC 51079-811
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101104
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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