Package 68071-3803-3

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 68071-3803-3
Digits Only 6807138033
Product NDC 68071-3803
Description

30 TABLET in 1 BOTTLE (68071-3803-3)

Marketing

Marketing Status
Marketed Since 2025-02-27
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": "2f27fabc-e7f1-055b-e063-6394a90a7315", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0368071380330"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["2f27f578-f965-04c9-e063-6394a90a1ae2"], "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": "30 TABLET in 1 BOTTLE (68071-3803-3)", "package_ndc": "68071-3803-3", "marketing_start_date": "20250227"}], "brand_name": "Allopurinol", "product_id": "68071-3803_2f27fabc-e7f1-055b-e063-6394a90a7315", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68071-3803", "generic_name": "Allopurinol", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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"}