Package 0054-0710-25

{"route": ["ORAL"], "spl_id": "32014633-5c89-4163-9fa7-239777c04d1d", "openfda": {"upc": ["0300540709259", "0300540710255"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["50f14803-78c0-4d19-8b5d-9a9c17582ac1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0054-0710-20)  / 100 TABLET in 1 BLISTER PACK", "package_ndc": "0054-0710-20", "marketing_start_date": "19830308"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0054-0710-25)", "package_ndc": "0054-0710-25", "marketing_start_date": "19830308"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "0054-0710_32014633-5c89-4163-9fa7-239777c04d1d", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-0710", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088109", "marketing_category": "ANDA", "marketing_start_date": "19830308", "listing_expiration_date": "20271231"}