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GlipizideER - 63629-3158-3 - (Glipizide)

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Drug Information of GlipizideER

Product NDC: 63629-3158
Proprietary Name: GlipizideER
Non Proprietary Name: Glipizide
Active Ingredient(s): 10    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of GlipizideER

Product NDC: 63629-3158
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076467
Marketing Category: ANDA
Start Marketing Date: 20031107

Package Information of GlipizideER

Package NDC: 63629-3158-3
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3158-3)

NDC Information of GlipizideER

NDC Code 63629-3158-3
Proprietary Name GlipizideER
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3158-3)
Product NDC 63629-3158
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20031107
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of GlipizideER


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