Package 68788-8865-1

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 68788-8865-1
Digits Only 6878888651
Product NDC 68788-8865
Description

100 TABLET in 1 BOTTLE (68788-8865-1)

Marketing

Marketing Status
Marketed Since 2025-04-23
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": "09d34fab-250c-496a-93f5-c8d9f52a2276", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["09d34fab-250c-496a-93f5-c8d9f52a2276"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8865-1)", "package_ndc": "68788-8865-1", "marketing_start_date": "20250423"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8865-3)", "package_ndc": "68788-8865-3", "marketing_start_date": "20250423"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8865-6)", "package_ndc": "68788-8865-6", "marketing_start_date": "20250423"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8865-9)", "package_ndc": "68788-8865-9", "marketing_start_date": "20250423"}], "brand_name": "ALLOPURINOL", "product_id": "68788-8865_09d34fab-250c-496a-93f5-c8d9f52a2276", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68788-8865", "generic_name": "ALLOPURINOL", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALLOPURINOL", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA217748", "marketing_category": "ANDA", "marketing_start_date": "20250423", "listing_expiration_date": "20261231"}