Package 76420-536-30

{"route": ["ORAL"], "spl_id": "f4ca3781-8aec-9696-e053-2a95a90adf9f", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709", "833711", "833713"], "spl_set_id": ["a26ca887-e26c-4c32-8dbd-1fa2eb6db9dc"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-30)", "package_ndc": "76420-536-30", "marketing_start_date": "20230216"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-60)", "package_ndc": "76420-536-60", "marketing_start_date": "20230216"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-90)", "package_ndc": "76420-536-90", "marketing_start_date": "20230216"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "76420-536_f4ca3781-8aec-9696-e053-2a95a90adf9f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-536", "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": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20261231"}