Glipizide - 49999-108-60 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 49999-108
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: 49999-108
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074305
Marketing Category: ANDA
Start Marketing Date: 19950407

Package Information of Glipizide

Package NDC: 49999-108-60
Package Description: 60 TABLET in 1 BOTTLE (49999-108-60)

NDC Information of Glipizide

NDC Code 49999-108-60
Proprietary Name Glipizide
Package Description 60 TABLET in 1 BOTTLE (49999-108-60)
Product NDC 49999-108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950407
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name GLIPIZIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information