allopurinol
Generic: allopurinol
Labeler: st. mary's medical park pharmacyDrug Facts
Product Profile
Brand Name
allopurinol
Generic Name
allopurinol
Labeler
st. mary's medical park pharmacy
Dosage Form
TABLET
Routes
Active Ingredients
allopurinol 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60760-710
Product ID
60760-710_42de3b25-692a-eaff-e063-6294a90a0d21
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214443
Listing Expiration
2026-12-31
Marketing Start
2024-05-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60760710
Hyphenated Format
60760-710
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA214443 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (60760-710-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42de3b25-692a-eaff-e063-6294a90a0d21", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["42de3b18-a289-e49e-e063-6394a90a89d4"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-710-90)", "package_ndc": "60760-710-90", "marketing_start_date": "20251105"}], "brand_name": "Allopurinol", "product_id": "60760-710_42de3b25-692a-eaff-e063-6294a90a0d21", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "60760-710", "generic_name": "Allopurinol", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA214443", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}