Package 64380-718-01

{"route": ["ORAL"], "spl_id": "0f4caac6-033d-478b-87f4-a736c902e532", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["24152345-b761-4f22-81a9-83a2b278a267"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64380-718-01)", "package_ndc": "64380-718-01", "marketing_start_date": "20250601"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64380-718-02)", "package_ndc": "64380-718-02", "marketing_start_date": "20250601"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64380-718-03)", "package_ndc": "64380-718-03", "marketing_start_date": "20250601"}], "brand_name": "tramadol hydrochloride", "product_id": "64380-718_0f4caac6-033d-478b-87f4-a736c902e532", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64380-718", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tramadol hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA202075", "marketing_category": "ANDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}