Glipizide - 0378-1105-05 - (glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 0378-1105
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: 0378-1105
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074226
Marketing Category: ANDA
Start Marketing Date: 20120531

Package Information of Glipizide

Package NDC: 0378-1105-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0378-1105-05)

NDC Information of Glipizide

NDC Code 0378-1105-05
Proprietary Name Glipizide
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0378-1105-05)
Product NDC 0378-1105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120531
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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