Package 68094-047-10

{"route": ["INTRAVENOUS"], "spl_id": "721350a6-f9ae-4c06-b8b5-41169d7cd43e", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718900", "1718906", "1718909"], "spl_set_id": ["e9d5c989-ebf6-4377-9c6e-7aef848a03a1"], "manufacturer_name": ["Precision Dose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (68094-047-10)  / 20 mL in 1 VIAL (68094-047-01)", "package_ndc": "68094-047-10", "marketing_start_date": "20201123"}], "brand_name": "Dexmedetomidine Hydrochloride in Sodium Chloride", "product_id": "68094-047_721350a6-f9ae-4c06-b8b5-41169d7cd43e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "68094-047", "generic_name": "Dexmedetomidine Hydrochloride", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine Hydrochloride in Sodium Chloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA212857", "marketing_category": "ANDA", "marketing_start_date": "20201123", "listing_expiration_date": "20261231"}