NDC 60429-181

Allopurinol

Allopurinol

Allopurinol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Golden State Medical Supply, Inc.. The primary component is Allopurinol.

Product ID60429-181_7cd6d025-f5d4-07a8-e053-2991aa0a3f51
NDC60429-181
Product TypeHuman Prescription Drug
Proprietary NameAllopurinol
Generic NameAllopurinol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-02-09
Marketing CategoryANDA / ANDA
Application NumberANDA071587
Labeler NameGolden State Medical Supply, Inc.
Substance NameALLOPURINOL
Active Ingredient Strength300 mg/1
Pharm ClassesXanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 60429-181-05

500 TABLET in 1 BOTTLE (60429-181-05)
Marketing Start Date2015-02-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60429-181-05 [60429018105]

Allopurinol TABLET
Marketing CategoryANDA
Application NumberANDA071587
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-02-20
Marketing End Date2018-12-31

NDC 60429-181-90 [60429018190]

Allopurinol TABLET
Marketing CategoryANDA
Application NumberANDA071587
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-02-20
Marketing End Date2018-01-31

NDC 60429-181-01 [60429018101]

Allopurinol TABLET
Marketing CategoryANDA
Application NumberANDA071587
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-02-20
Marketing End Date2018-01-31

Drug Details

Active Ingredients

IngredientStrength
ALLOPURINOL300 mg/1

OpenFDA Data

SPL SET ID:f254fc9a-0740-4a31-82be-6405cbd6cda6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197320
  • 197319

    • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    0378-0137Allopurinolallopurinol
    0378-0181Allopurinolallopurinol
    0591-5543AllopurinolAllopurinol
    0591-5544AllopurinolAllopurinol
    0603-2115Allopurinolallopurinol
    0603-2116Allopurinolallopurinol
    0615-1592AllopurinolAllopurinol
    0615-1593AllopurinolAllopurinol
    0615-8321AllopurinolAllopurinol
    0615-8385Allopurinolallopurinol
    0904-6571Allopurinolallopurinol
    0904-6572Allopurinolallopurinol
    0904-7041AllopurinolAllopurinol
    10544-545AllopurinolAllopurinol
    10544-547AllopurinolAllopurinol
    10544-911AllopurinolAllopurinol
    16571-883Allopurinolallopurinol
    16571-884Allopurinolallopurinol
    16571-885Allopurinolallopurinol
    16714-041AllopurinolAllopurinol
    16714-042AllopurinolAllopurinol
    67544-988AllopurinolAllopurinol
    68071-4131AllopurinolAllopurinol
    68788-6422AllopurinolAllopurinol
    68788-2115AllopurinolAllopurinol
    68788-0603AllopurinolAllopurinol
    68788-6323AllopurinolAllopurinol
    68788-7383AllopurinolAllopurinol
    68788-9331AllopurinolAllopurinol
    68788-9831AllopurinolAllopurinol
    68788-9832AllopurinolAllopurinol
    70518-0429AllopurinolAllopurinol
    70518-0451AllopurinolAllopurinol
    70518-0190AllopurinolAllopurinol
    70518-0476AllopurinolAllopurinol
    70518-0555AllopurinolAllopurinol
    70518-1576AllopurinolAllopurinol
    70518-1678AllopurinolAllopurinol
    70518-1407AllopurinolAllopurinol
    70518-1573AllopurinolAllopurinol
    70710-1209AllopurinolAllopurinol
    70518-1806AllopurinolAllopurinol
    70771-1127AllopurinolAllopurinol
    70710-1210AllopurinolAllopurinol
    70771-1126AllopurinolAllopurinol
    71205-049AllopurinolAllopurinol
    70934-072AllopurinolAllopurinol
    71335-0599AllopurinolAllopurinol
    71335-0112AllopurinolAllopurinol
    71335-0467AllopurinolAllopurinol
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.