NDC 53217-187

Allopurinol

Allopurinol

Allopurinol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aidarex Pharmaceuticals Llc. The primary component is Allopurinol.

Product ID53217-187_2ca799ba-56af-4fa6-ac9c-44f736ef1a02
NDC53217-187
Product TypeHuman Prescription Drug
Proprietary NameAllopurinol
Generic NameAllopurinol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-04-06
Marketing CategoryNDA / NDA
Application NumberNDA018832
Labeler NameAidarex Pharmaceuticals LLC
Substance NameALLOPURINOL
Active Ingredient Strength100 mg/1
Pharm ClassesXanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 53217-187-60

60 TABLET in 1 BOTTLE (53217-187-60)
Marketing Start Date2009-04-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53217-187-90 [53217018790]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-04-06
Inactivation Date2020-01-31

NDC 53217-187-30 [53217018730]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-04-06
Inactivation Date2020-01-31

NDC 53217-187-60 [53217018760]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-04-06
Inactivation Date2020-01-31

NDC 53217-187-00 [53217018700]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018832
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-04-06
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALLOPURINOL100 mg/1

OpenFDA Data

SPL SET ID:c9a01871-bbf8-4b31-9b9b-9fa8c0997b29
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 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.