Package 27808-301-01

{"route": ["ORAL"], "spl_id": "18541c83-30aa-4df4-9d72-915629ee01f9", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["1d4af58f-17f3-4cbd-870c-098ace954872"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (27808-301-01)", "package_ndc": "27808-301-01", "marketing_start_date": "20241222"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (27808-301-02)", "package_ndc": "27808-301-02", "marketing_start_date": "20241222"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (27808-301-03)", "package_ndc": "27808-301-03", "marketing_start_date": "20241222"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "27808-301_18541c83-30aa-4df4-9d72-915629ee01f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "27808-301", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA091498", "marketing_category": "ANDA", "marketing_start_date": "20241222", "listing_expiration_date": "20261231"}