NDC 71335-0039

Glipizide

Glipizide

Glipizide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Glipizide.

Product ID71335-0039_0f25675d-f851-4108-a1e7-3d0819feb6f4
NDC71335-0039
Product TypeHuman Prescription Drug
Proprietary NameGlipizide
Generic NameGlipizide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-07-18
Marketing CategoryANDA / ANDA
Application NumberANDA074550
Labeler NameBryant Ranch Prepack
Substance NameGLIPIZIDE
Active Ingredient Strength10 mg/1
Pharm ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71335-0039-1

60 TABLET in 1 BOTTLE (71335-0039-1)
Marketing Start Date2011-07-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0039-2 [71335003902]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

NDC 71335-0039-5 [71335003905]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

NDC 71335-0039-4 [71335003904]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

NDC 71335-0039-7 [71335003907]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

NDC 71335-0039-3 [71335003903]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

NDC 71335-0039-6 [71335003906]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

NDC 71335-0039-1 [71335003901]

Glipizide TABLET
Marketing CategoryANDA
Application NumberANDA074550
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-07-18

Drug Details

Active Ingredients

IngredientStrength
GLIPIZIDE10 mg/1

OpenFDA Data

SPL SET ID:464f4284-556f-432f-9f9f-b1dff3520358
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310490
  • 310488

    • Pharmacological Class

    • Sulfonylurea [EPC]
    • Sulfonylurea Compounds [CS]

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

    NDCBrand NameGeneric Name
    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
    68071-1773GlipizideGlipizide
    68071-3009GlipizideGlipizide
    68071-3141GlipizideGlipizide
    68071-4223GlipizideGlipizide
    68071-4124GlipizideGlipizide
    68071-4085GlipizideGlipizide
    68071-4378GlipizideGlipizide
    68071-4498GlipizideGlipizide
    68071-4020GlipizideGlipizide
    68071-4232GlipizideGlipizide
    68071-4643GlipizideGlipizide
    68382-337GlipizideGlipizide
    68382-336GlipizideGlipizide
    68382-335GlipizideGlipizide
    68645-575GlipizideGlipizide
    68788-0141GlipizideGlipizide
    68645-151GlipizideGlipizide
    68645-574GlipizideGlipizide
    68788-0142GlipizideGlipizide
    68788-7250GlipizideGlipizide
    68788-6853GlipizideGlipizide
    68788-6854GlipizideGlipizide
    68788-9176GlipizideGlipizide
    68788-7230GlipizideGlipizide
    68788-9918GlipizideGlipizide
    70518-0029GlipizideGlipizide
    70518-0104GlipizideGlipizide
    70518-0552GlipizideGlipizide
    70518-0115GlipizideGlipizide
    70518-0389GlipizideGlipizide
    70518-0358GlipizideGlipizide
    70518-1124GlipizideGlipizide
    70518-0998GlipizideGlipizide
    70518-1063GlipizideGlipizide
    70518-0574GlipizideGlipizide
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.