Package 0904-6572-61

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 0904-6572-61
Digits Only 0904657261
Product NDC 0904-6572
Product ID 0904-6572_e8995c18-7672-418d-8e39-bffe2ad7c7fb
Description

100 BLISTER PACK in 1 CARTON (0904-6572-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2003-06-27
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": "e8995c18-7672-418d-8e39-bffe2ad7c7fb", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["8c0f5af5-a453-4641-933f-ccb2625fca39"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6572-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6572-61", "marketing_start_date": "20030627"}], "brand_name": "Allopurinol", "product_id": "0904-6572_e8995c18-7672-418d-8e39-bffe2ad7c7fb", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0904-6572", "generic_name": "allopurinol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA075798", "marketing_category": "ANDA", "marketing_start_date": "20030627", "listing_expiration_date": "20261231"}