Glipizide - 55289-806-14 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 55289-806
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: 55289-806
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 19950227

Package Information of Glipizide

Package NDC: 55289-806-14
Package Description: 14 TABLET in 1 BOTTLE, PLASTIC (55289-806-14)

NDC Information of Glipizide

NDC Code 55289-806-14
Proprietary Name Glipizide
Package Description 14 TABLET in 1 BOTTLE, PLASTIC (55289-806-14)
Product NDC 55289-806
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 PD-Rx 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