Package 55111-730-05

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 55111-730-05
Digits Only 5511173005
Product NDC 55111-730
Description

500 TABLET in 1 BOTTLE (55111-730-05)

Marketing

Marketing Status
Marketed Since 2009-10-01
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": "c3be239e-a0b5-fb8d-2ae6-372cef6fa362", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0355111729013", "0355111730019"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["19a138b8-d225-03e6-f762-abe71560204b"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-730-01)", "package_ndc": "55111-730-01", "marketing_start_date": "20091001"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-730-05)", "package_ndc": "55111-730-05", "marketing_start_date": "20091001"}], "brand_name": "Allopurinol", "product_id": "55111-730_c3be239e-a0b5-fb8d-2ae6-372cef6fa362", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "55111-730", "generic_name": "allopurinol", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA071587", "marketing_category": "ANDA", "marketing_start_date": "20091001", "listing_expiration_date": "20261231"}