NDC 71335-0484

Glimepiride

Glimepiride

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

Product ID71335-0484_1a3ec24e-5b38-4f29-ad7a-2f28ea639d3b
NDC71335-0484
Product TypeHuman Prescription Drug
Proprietary NameGlimepiride
Generic NameGlimepiride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-08-23
Marketing CategoryANDA / ANDA
Application NumberANDA078181
Labeler NameBryant Ranch Prepack
Substance NameGLIMEPIRIDE
Active Ingredient Strength2 mg/1
Pharm ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-0484-1

30 TABLET in 1 BOTTLE (71335-0484-1)
Marketing Start Date2015-01-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0484-3 [71335048403]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-31
Marketing End Date2019-05-31

NDC 71335-0484-4 [71335048404]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-31
Marketing End Date2019-05-31

NDC 71335-0484-1 [71335048401]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-31
Marketing End Date2019-05-31

NDC 71335-0484-5 [71335048405]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-31
Marketing End Date2019-05-31

NDC 71335-0484-2 [71335048402]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-31
Marketing End Date2019-05-31

Drug Details

Active Ingredients

IngredientStrength
GLIMEPIRIDE2 mg/1

OpenFDA Data

SPL SET ID:9e863f84-d6f2-4d61-8250-774569e84353
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199247
  • 199246

    • Pharmacological Class

    • Sulfonylurea [EPC]
    • Sulfonylurea Compounds [CS]

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

    NDCBrand NameGeneric Name
    0093-7254GlimepirideGlimepiride
    0093-7255GlimepirideGlimepiride
    0093-7256GlimepirideGlimepiride
    0378-4011Glimepirideglimepiride
    0378-4012Glimepirideglimepiride
    0378-4013Glimepirideglimepiride
    0440-6564GlimepirideGlimepiride
    0440-6565GlimepirideGlimepiride
    0440-6566GlimepirideGlimepiride
    0615-6575GlimepirideGlimepiride
    0615-6576GlimepirideGlimepiride
    0615-7523GlimepirideGlimepiride
    0615-8332GlimepirideGlimepiride
    0615-8333GlimepirideGlimepiride
    0615-8334GlimepirideGlimepiride
    10544-217GlimepirideGlimepiride
    10544-219GlimepirideGlimepiride
    16571-773GlimepirideGlimepiride
    16571-774GlimepirideGlimepiride
    16571-775GlimepirideGlimepiride
    16729-001GlimepirideGlimepiride
    16729-002GlimepirideGlimepiride
    16729-003GlimepirideGlimepiride
    21695-746GlimepirideGlimepiride
    21695-747GlimepirideGlimepiride
    21695-993GlimepirideGlimepiride
    33261-831GlimepirideGlimepiride
    33261-892GlimepirideGlimepiride
    33261-961GlimepirideGlimepiride
    35356-896GlimepirideGlimepiride
    42571-100GlimepirideGlimepiride
    68001-179GlimepirideGlimepiride
    68001-177GlimepirideGlimepiride
    68001-178GlimepirideGlimepiride
    68071-1942GlimepirideGlimepiride
    68071-1910GlimepirideGlimepiride
    68071-3024GlimepirideGlimepiride
    68071-1991GlimepirideGlimepiride
    68071-3068GlimepirideGlimepiride
    68071-3239GlimepirideGlimepiride
    68084-327GlimepirideGlimepiride
    68084-326GlimepirideGlimepiride
    68084-788GlimepirideGlimepiride
    68645-572GlimepirideGlimepiride
    68645-573GlimepirideGlimepiride
    68788-6801GlimepirideGlimepiride
    68788-6818GlimepirideGlimepiride
    68788-6436GlimepirideGlimepiride
    68788-6411GlimepirideGlimepiride
    69452-129GlimepirideGlimepiride
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