Package 60760-772-50

{"route": ["ORAL"], "spl_id": "f3bf6f98-f388-3249-e053-2995a90a2fbb", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["f2f421ab-35ae-7637-e053-2995a90a40e0"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-772-09)", "package_ndc": "60760-772-09", "marketing_start_date": "20221228"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-772-20)", "package_ndc": "60760-772-20", "marketing_start_date": "20230202"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-772-30)", "package_ndc": "60760-772-30", "marketing_start_date": "20221228"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-772-50)", "package_ndc": "60760-772-50", "marketing_start_date": "20230202"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-772-60)", "package_ndc": "60760-772-60", "marketing_start_date": "20230202"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-772-90)", "package_ndc": "60760-772-90", "marketing_start_date": "20230202"}], "brand_name": "Tramadol Hydrochloride", "product_id": "60760-772_f3bf6f98-f388-3249-e053-2995a90a2fbb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-772", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA203494", "marketing_category": "ANDA", "marketing_start_date": "20221228", "listing_expiration_date": "20261231"}