NDC 63629-4071

Glipizide ER

Glipizide

Glipizide ER is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Glipizide.

Product ID63629-4071_92366bf9-30e6-4f7e-b7bc-1787d5852d75
NDC63629-4071
Product TypeHuman Prescription Drug
Proprietary NameGlipizide ER
Generic NameGlipizide
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2003-11-19
Marketing CategoryANDA / ANDA
Application NumberANDA076467
Labeler NameBryant Ranch Prepack
Substance NameGLIPIZIDE
Active Ingredient Strength5 mg/1
Pharm ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63629-4071-4

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4071-4)
Marketing Start Date2009-09-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-4071-4 [63629407104]

Glipizide ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076467
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-10
Inactivation Date2020-01-31

NDC 63629-4071-3 [63629407103]

Glipizide ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076467
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-10
Inactivation Date2020-01-31

NDC 63629-4071-2 [63629407102]

Glipizide ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076467
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-10
Inactivation Date2020-01-31

NDC 63629-4071-1 [63629407101]

Glipizide ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076467
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-10
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
GLIPIZIDE5 mg/1

OpenFDA Data

SPL SET ID:760d589c-24f1-c89a-bc01-ea57101b2f20
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314006
  • Pharmacological Class

    • Sulfonylurea [EPC]
    • Sulfonylurea Compounds [CS]

    NDC Crossover Matching brand name "Glipizide ER" or generic name "Glipizide"

    NDCBrand NameGeneric Name
    68071-1557Glipizide ERGlipizide ER
    68071-2181Glipizide ERGlipizide ER
    68071-1944Glipizide ERGlipizide ER
    68071-4010Glipizide ERGlipizide ER
    68071-4133Glipizide ERGlipizide ER
    68084-112Glipizide ERGlipizide ER
    68084-111Glipizide ERGlipizide ER
    68084-295Glipizide ERGlipizide ER
    68151-0765Glipizide ERGlipizide ER
    70518-0827Glipizide ERGlipizide ER
    70518-0288Glipizide ERGlipizide ER
    70518-0456Glipizide ERGlipizide ER
    21695-967Glipizide ERGlipizide ER
    50090-2222Glipizide ERGlipizide ER
    50436-6302Glipizide ERGlipizide ER
    50436-0908Glipizide ERGlipizide ER
    53808-0401Glipizide ERGlipizide ER
    55289-301Glipizide ERGlipizide ER
    55289-779Glipizide ERGlipizide ER
    61919-725GLIPIZIDE ERGLIPIZIDE ER
    63629-5256Glipizide ERGlipizide ER
    63629-3158Glipizide ERGlipizide ER
    63629-7093Glipizide ERGlipizide ER
    63629-4071Glipizide ERGlipizide ER
    66336-269Glipizide ERGlipizide ER
    61919-850GLIPIZIDE ERGLIPIZIDE ER
    70518-2579Glipizide ERGlipizide ER
    70518-2549Glipizide ERGlipizide ER
    50090-0852Glipizide ERGlipizide ER
    72189-070GLIPIZIDE ERGLIPIZIDE ER
    0378-1105Glipizideglipizide
    0378-1110Glipizideglipizide
    0591-0460GlipizideGlipizide
    0591-0461GlipizideGlipizide
    0591-0844GlipizideGlipizide
    0591-0845GlipizideGlipizide
    0591-0900GlipizideGlipizide
    0615-3595GlipizideGlipizide
    0615-3596GlipizideGlipizide
    0615-5584GlipizideGlipizide
    0615-5585GlipizideGlipizide
    0615-6596GlipizideGlipizide
    0615-7968GlipizideGlipizide
    0615-7969GlipizideGlipizide
    0615-8407GlipizideGlipizide
    0049-0170Glucotrolglipizide
    0049-0174Glucotrolglipizide
    0049-0178Glucotrolglipizide
    0049-4110Glucotrolglipizide
    0049-4120Glucotrolglipizide

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