Package 68071-3605-9
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
68071-3605-9
Digits Only
6807136059
Product NDC
68071-3605
Description
90 TABLET in 1 BOTTLE (68071-3605-9)
Marketing
Marketing Status
Brand
allopurinol
Generic
allopurinol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b1c6812-0802-5b1c-e063-6294a90a9f9f", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0368071360592"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["1b1c5cde-b2ed-ebc8-e063-6394a90a66c6"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3605-9)", "package_ndc": "68071-3605-9", "marketing_start_date": "20240617"}], "brand_name": "Allopurinol", "product_id": "68071-3605_1b1c6812-0802-5b1c-e063-6294a90a9f9f", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68071-3605", "generic_name": "Allopurinol", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20200922", "listing_expiration_date": "20261231"}