NDC 62332-190

Febuxostat

Febuxostat

Febuxostat is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is Febuxostat.

Product ID62332-190_7ed339c2-dd58-4cbd-9fdc-47149c2f6903
NDC62332-190
Product TypeHuman Prescription Drug
Proprietary NameFebuxostat
Generic NameFebuxostat
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2019-07-01
Marketing CategoryANDA / ANDA
Application NumberANDA205421
Labeler NameAlembic Pharmaceuticals Inc.
Substance NameFEBUXOSTAT
Active Ingredient Strength40 mg/1
Pharm ClassesXanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 62332-190-08

80 TABLET, COATED in 1 CARTON (62332-190-08)
Marketing Start Date2019-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62332-190-30 [62332019030]

Febuxostat TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205421
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-07-01

NDC 62332-190-08 [62332019008]

Febuxostat TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205421
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-01

NDC 62332-190-10 [62332019010]

Febuxostat TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205421
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-01

NDC 62332-190-31 [62332019031]

Febuxostat TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205421
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-01

NDC 62332-190-91 [62332019091]

Febuxostat TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205421
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-01

Drug Details

Active Ingredients

IngredientStrength
FEBUXOSTAT40 mg/1

OpenFDA Data

SPL SET ID:9a87099f-d82d-42c7-872a-b87d3917e960
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 834241
  • 834235
    • UPC Code
  • 0362332190300
  • 0362332191307

    • Pharmacological Class

    • Xanthine Oxidase Inhibitor [EPC]
    • Xanthine Oxidase Inhibitors [MoA]
    • Xanthine Oxidase Inhibitor [EPC]
    • Xanthine Oxidase Inhibitors [MoA]

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

    NDCBrand NameGeneric Name
    0054-0413FebuxostatFebuxostat
    0054-0414FebuxostatFebuxostat
    0378-3925Febuxostatfebuxostat
    0378-3926Febuxostatfebuxostat
    0527-2244FEBUXOSTATfebuxostat
    0527-2248FEBUXOSTATfebuxostat
    14445-156FebuxostatFebuxostat
    14445-157FebuxostatFebuxostat
    16714-059FebuxostatFebuxostat
    16714-060FebuxostatFebuxostat
    27808-206Febuxostatfebuxostat
    27808-207Febuxostatfebuxostat
    43547-295FEBUXOSTATfebuxostat
    43547-296FEBUXOSTATfebuxostat
    46708-190Febuxostatfebuxostat
    46708-191Febuxostatfebuxostat
    47335-721FebuxostatFebuxostat
    47335-722FebuxostatFebuxostat
    48792-7905FEBUXOSTATfebuxostat
    48792-7906FEBUXOSTATfebuxostat
    51407-293FebuxostatFebuxostat
    51407-294FebuxostatFebuxostat
    55111-796FebuxostatFebuxostat
    55111-797FebuxostatFebuxostat
    60687-538FebuxostatFebuxostat
    62332-190Febuxostatfebuxostat
    62332-191Febuxostatfebuxostat
    63304-864FebuxostatFebuxostat
    63304-865FebuxostatFebuxostat
    69539-036FebuxostatFebuxostat
    69539-035FebuxostatFebuxostat
    71610-386FebuxostatFebuxostat
    71610-411FebuxostatFebuxostat
    72205-028FebuxostatFebuxostat
    72205-029FebuxostatFebuxostat
    71610-450FebuxostatFebuxostat
    68071-5271FebuxostatFebuxostat
    21695-516ULORICfebuxostat
    43353-305ULORICfebuxostat
    55154-5158ULORICfebuxostat
    55154-5159ULORICfebuxostat
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.