GLIPIZIDE - 16590-287-82 - (GLIPIZIDE)

Alphabetical Index


Drug Information of GLIPIZIDE

Product NDC: 16590-287
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: 16590-287
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19950227

Package Information of GLIPIZIDE

Package NDC: 16590-287-82
Package Description: 180 TABLET in 1 BOTTLE (16590-287-82)

NDC Information of GLIPIZIDE

NDC Code 16590-287-82
Proprietary Name GLIPIZIDE
Package Description 180 TABLET in 1 BOTTLE (16590-287-82)
Product NDC 16590-287
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 STAT Rx USA LLC
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of GLIPIZIDE


General Information