NDC 50742-136

Allopurinol

Allopurinol

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

Product ID50742-136_457d1969-77ba-47c3-904e-95b1b3fa1db2
NDC50742-136
Product TypeHuman Prescription Drug
Proprietary NameAllopurinol
Generic NameAllopurinol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-08-08
Marketing CategoryANDA / ANDA
Application NumberANDA204467
Labeler NameIngenus Pharmaceuticals LLC
Substance NameALLOPURINOL
Active Ingredient Strength300 mg/1
Pharm ClassesXanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50742-136-05

500 TABLET in 1 BOTTLE (50742-136-05)
Marketing Start Date2016-08-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50742-136-10 [50742013610]

Allopurinol TABLET
Marketing CategoryEXPORT ONLY
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-08-08
Marketing End Date2019-12-03

NDC 50742-136-01 [50742013601]

Allopurinol TABLET
Marketing CategoryEXPORT ONLY
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-08-08
Marketing End Date2019-12-03

NDC 50742-136-05 [50742013605]

Allopurinol TABLET
Marketing CategoryEXPORT ONLY
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-08-08
Marketing End Date2019-12-03

Drug Details

Active Ingredients

IngredientStrength
ALLOPURINOL300 mg/1

OpenFDA Data

SPL SET ID:4a67786e-57d5-4e03-9d99-97a3a2b1670f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197320
  • 197319
  • UPC Code
  • 0350742135103
  • Pharmacological Class

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

    Medicade Reported Pricing

    50742013605 ALLOPURINOL 300 MG TABLET

    Pricing Unit: EA | Drug Type:

    50742013601 ALLOPURINOL 300 MG TABLET

    Pricing Unit: EA | Drug Type:

    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.