Package 68071-3871-1

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 68071-3871-1
Digits Only 6807138711
Product NDC 68071-3871
Description

100 TABLET in 1 BOTTLE (68071-3871-1)

Marketing

Marketing Status
Marketed Since 2025-06-23
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": "3845bbfe-6642-bf56-e063-6294a90ae3e2", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0368071387117"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["3845c310-099b-8e11-e063-6394a90abd2f"], "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": "100 TABLET in 1 BOTTLE (68071-3871-1)", "package_ndc": "68071-3871-1", "marketing_start_date": "20250623"}], "brand_name": "Allopurinol", "product_id": "68071-3871_3845bbfe-6642-bf56-e063-6294a90ae3e2", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68071-3871", "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": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}