Package 64980-614-01

{"route": ["ORAL"], "spl_id": "647eea85-16ed-4f3c-89ef-c2e41d37a1dc", "openfda": {"upc": ["0364980663014"], "unii": ["9N7R477WCK"], "rxcui": ["835603", "2179635"], "spl_set_id": ["b5852b90-e415-47ef-8f73-87266b58e033"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-614-01)", "package_ndc": "64980-614-01", "marketing_start_date": "20240805"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64980-614-10)", "package_ndc": "64980-614-10", "marketing_start_date": "20240805"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64980-614-50)", "package_ndc": "64980-614-50", "marketing_start_date": "20240805"}], "brand_name": "Tramadol Hydrochloride", "product_id": "64980-614_647eea85-16ed-4f3c-89ef-c2e41d37a1dc", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64980-614", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075968", "marketing_category": "ANDA", "marketing_start_date": "20240805", "listing_expiration_date": "20261231"}