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Glucotrol XL - 54868-3335-3 - (glipizide)

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Drug Information of Glucotrol XL

Product NDC: 54868-3335
Proprietary Name: Glucotrol XL
Non Proprietary Name: glipizide
Active Ingredient(s): 5    mg/1 & nbsp;   glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Glucotrol XL

Product NDC: 54868-3335
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020329
Marketing Category: NDA
Start Marketing Date: 19940801

Package Information of Glucotrol XL

Package NDC: 54868-3335-3
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-3335-3)

NDC Information of Glucotrol XL

NDC Code 54868-3335-3
Proprietary Name Glucotrol XL
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-3335-3)
Product NDC 54868-3335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glipizide
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19940801
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name GLIPIZIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glucotrol XL


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