Package 70752-139-06

{"route": ["ORAL"], "spl_id": "ea7f15a6-079d-4146-a13d-74c129ec598e", "openfda": {"upc": ["0370752139120"], "unii": ["GSL05Y1MN6", "R61ZEH7I1I"], "rxcui": ["991486"], "spl_set_id": ["9aca56ec-28f8-4679-9f90-ec3e82deb9ac"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (70752-139-06)", "package_ndc": "70752-139-06", "marketing_start_date": "20201008"}, {"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (70752-139-12)", "package_ndc": "70752-139-12", "marketing_start_date": "20201008"}], "brand_name": "Promethazine Hydrochloride and Codeine Phosphate", "product_id": "70752-139_ea7f15a6-079d-4146-a13d-74c129ec598e", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]", "Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70752-139", "dea_schedule": "CV", "generic_name": "Promethazine Hydrochloride and Codeine Phosphate", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride and Codeine Phosphate", "active_ingredients": [{"name": "CODEINE PHOSPHATE", "strength": "10 mg/5mL"}, {"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "6.25 mg/5mL"}], "application_number": "ANDA214238", "marketing_category": "ANDA", "marketing_start_date": "20201008", "listing_expiration_date": "20261231"}