Package 68071-3672-9

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 68071-3672-9
Digits Only 6807136729
Product NDC 68071-3672
Description

90 TABLET in 1 BOTTLE (68071-3672-9)

Marketing

Marketing Status
Marketed Since 2024-08-30
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": "20eef462-eda9-22b8-e063-6394a90adebc", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0368071367294"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["20eef55e-0d70-874b-e063-6394a90aa06a"], "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 (68071-3672-9)", "package_ndc": "68071-3672-9", "marketing_start_date": "20240830"}], "brand_name": "Allopurinol", "product_id": "68071-3672_20eef462-eda9-22b8-e063-6394a90adebc", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68071-3672", "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": "ANDA214443", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}