allopurinol

Generic: allopurinol

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 16714-576
Product ID 16714-576_0f560d11-3ba5-4dd4-8c20-ed9b43bfd69a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204467
Listing Expiration 2026-12-31
Marketing Start 2022-07-01

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 16714576
Hyphenated Format 16714-576

Supplemental Identifiers

RxCUI
197319 197320
UPC
0316714576046 0316714576022 0316714577012 0316714576039 0316714577029 0316714576015
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 ANDA204467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (16714-576-01)
  • 100 TABLET in 1 BOTTLE (16714-576-02)
  • 500 TABLET in 1 BOTTLE (16714-576-03)
  • 1000 TABLET in 1 BOTTLE (16714-576-04)
source: ndc

Packages (4)

16714-576-01 30 TABLET in 1 BOTTLE (16714-576-01) 16714-576-02 100 TABLET in 1 BOTTLE (16714-576-02) 16714-576-03 500 TABLET in 1 BOTTLE (16714-576-03) 16714-576-04 1000 TABLET in 1 BOTTLE (16714-576-04)

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": "0f560d11-3ba5-4dd4-8c20-ed9b43bfd69a", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0316714576046", "0316714576022", "0316714577012", "0316714576039", "0316714577029", "0316714576015"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["95a1ca8c-9855-4b11-92cd-6fdc144f0d3b"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (16714-576-01)", "package_ndc": "16714-576-01", "marketing_start_date": "20220701"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-576-02)", "package_ndc": "16714-576-02", "marketing_start_date": "20220701"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16714-576-03)", "package_ndc": "16714-576-03", "marketing_start_date": "20220701"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16714-576-04)", "package_ndc": "16714-576-04", "marketing_start_date": "20220701"}], "brand_name": "Allopurinol", "product_id": "16714-576_0f560d11-3ba5-4dd4-8c20-ed9b43bfd69a", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "16714-576", "generic_name": "Allopurinol", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}