Package 51655-968-52

{"route": ["ORAL"], "spl_id": "4974bd34-840b-e896-e063-6394a90a41e9", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["df745f5f-7f05-205d-e053-2995a90a05a4"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-968-26)", "package_ndc": "51655-968-26", "marketing_start_date": "20220602"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-968-52)", "package_ndc": "51655-968-52", "marketing_start_date": "20220408"}], "brand_name": "Allopurinol", "product_id": "51655-968_4974bd34-840b-e896-e063-6394a90a41e9", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "51655-968", "generic_name": "Allopurinol", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA071450", "marketing_category": "ANDA", "marketing_start_date": "20220408", "listing_expiration_date": "20271231"}