allopurinol

Generic: allopurinol

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 200 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-884
Product ID 16571-884_5cd32f4f-2795-4776-ad00-f33f91bda391
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA016084
Listing Expiration 2026-12-31
Marketing Start 2023-09-21

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 16571884
Hyphenated Format 16571-884

Supplemental Identifiers

RxCUI
197319 197320 245422
UPC
0316571885091 0316571884094 0316571883097
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

Packaging Origin

Original Packager
true

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 NDA016084 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16571-884-01)
  • 90 TABLET in 1 BOTTLE (16571-884-09)
  • 1000 TABLET in 1 BOTTLE (16571-884-10)
  • 500 TABLET in 1 BOTTLE (16571-884-50)
source: ndc

Packages (4)

16571-884-01 100 TABLET in 1 BOTTLE (16571-884-01) 16571-884-09 90 TABLET in 1 BOTTLE (16571-884-09) 16571-884-10 1000 TABLET in 1 BOTTLE (16571-884-10) 16571-884-50 500 TABLET in 1 BOTTLE (16571-884-50)

Ingredients (1)

allopurinol (200 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": "5cd32f4f-2795-4776-ad00-f33f91bda391", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0316571885091", "0316571884094", "0316571883097"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["30ad5ba2-1cef-4933-b104-0597f6a2aaa2"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-884-01)", "package_ndc": "16571-884-01", "marketing_start_date": "20230921"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (16571-884-09)", "package_ndc": "16571-884-09", "marketing_start_date": "20230921"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-884-10)", "package_ndc": "16571-884-10", "marketing_start_date": "20230921"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-884-50)", "package_ndc": "16571-884-50", "marketing_start_date": "20230921"}], "brand_name": "Allopurinol", "product_id": "16571-884_5cd32f4f-2795-4776-ad00-f33f91bda391", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "16571-884", "generic_name": "allopurinol", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "200 mg/1"}], "application_number": "NDA016084", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230921", "listing_expiration_date": "20261231"}