Package 0378-0181-05

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 0378-0181-05
Digits Only 0378018105
Product NDC 0378-0181
Product ID 0378-0181_38f49ed2-9641-404b-8146-5555064b86e8
Description

500 TABLET in 1 BOTTLE (0378-0181-05)

Marketing

Marketing Status
Marketed Since 1986-10-24
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (1)

Allopurinol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38f49ed2-9641-404b-8146-5555064b86e8", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["bdbf5ad4-86f2-4e9c-a51a-fb0c7220c480"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0378-0181-01)", "package_ndc": "0378-0181-01", "marketing_start_date": "19861024"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0378-0181-05)", "package_ndc": "0378-0181-05", "marketing_start_date": "19861024"}], "brand_name": "Allopurinol", "product_id": "0378-0181_38f49ed2-9641-404b-8146-5555064b86e8", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0378-0181", "generic_name": "allopurinol", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA018659", "marketing_category": "ANDA", "marketing_start_date": "19861024", "listing_expiration_date": "20261231"}