Package 76420-244-60

{"route": ["ORAL"], "spl_id": "e49bb4f0-8b07-c774-e053-2a95a90acff7", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709", "833711", "833713"], "spl_set_id": ["dce0d21e-e4c2-4875-a2ce-9d53df190b80"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-30)", "package_ndc": "76420-244-30", "marketing_start_date": "20220725"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-60)", "package_ndc": "76420-244-60", "marketing_start_date": "20220725"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-90)", "package_ndc": "76420-244-90", "marketing_start_date": "20220725"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "76420-244_e49bb4f0-8b07-c774-e053-2a95a90acff7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-244", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA201384", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}