allopurinol

Generic: allopurinol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7791
Product ID 50090-7791_f46ce49e-4667-4837-9d80-c37d143f27fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217748
Listing Expiration 2026-12-31
Marketing Start 2023-08-03

Pharmacologic Class

Established (EPC)
xanthine oxidase inhibitor [epc]
Mechanism of Action
xanthine oxidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907791
Hyphenated Format 50090-7791

Supplemental Identifiers

RxCUI
197319
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allopurinol (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number ANDA217748 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-7791-0)
  • 500 TABLET in 1 BOTTLE (50090-7791-1)
source: ndc

Packages (2)

50090-7791-0 100 TABLET in 1 BOTTLE (50090-7791-0) 50090-7791-1 500 TABLET in 1 BOTTLE (50090-7791-1)

Ingredients (1)

allopurinol (100 mg/1)

Linked Drug Pages (1)

ALLOPURINOL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f46ce49e-4667-4837-9d80-c37d143f27fc", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["8047206e-305b-44d2-aa61-dff0366e7675"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7791-0)", "package_ndc": "50090-7791-0", "marketing_start_date": "20251124"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50090-7791-1)", "package_ndc": "50090-7791-1", "marketing_start_date": "20251124"}], "brand_name": "ALLOPURINOL", "product_id": "50090-7791_f46ce49e-4667-4837-9d80-c37d143f27fc", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "50090-7791", "generic_name": "ALLOPURINOL", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALLOPURINOL", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA217748", "marketing_category": "ANDA", "marketing_start_date": "20230803", "listing_expiration_date": "20261231"}