allopurinol

Generic: allopurinol

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 300 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-688
Product ID 60687-688_351f1ba0-8015-9455-e063-6294a90a17a3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211820
Listing Expiration 2026-12-31
Marketing Start 2022-12-09

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 60687688
Hyphenated Format 60687-688

Supplemental Identifiers

RxCUI
197319 197320
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 ANDA211820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-688-01) / 1 TABLET in 1 BLISTER PACK (60687-688-11)
source: ndc

Packages (1)

60687-688-01 100 BLISTER PACK in 1 CARTON (60687-688-01) / 1 TABLET in 1 BLISTER PACK (60687-688-11)

Ingredients (1)

allopurinol (300 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": "351f1ba0-8015-9455-e063-6294a90a17a3", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["f6f7642b-5046-47d6-b259-0c9f8aed3b34"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-688-01)  / 1 TABLET in 1 BLISTER PACK (60687-688-11)", "package_ndc": "60687-688-01", "marketing_start_date": "20221209"}], "brand_name": "Allopurinol", "product_id": "60687-688_351f1ba0-8015-9455-e063-6294a90a17a3", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "60687-688", "generic_name": "Allopurinol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA211820", "marketing_category": "ANDA", "marketing_start_date": "20221209", "listing_expiration_date": "20261231"}