Package 70121-1711-9

{"route": ["INTRAVENOUS"], "spl_id": "4751c8c4-1971-44bb-8311-fea390cc1b98", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["4df8cc35-fc80-4438-b982-9c4b7d17bad2"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 POUCH in 1 CARTON (70121-1711-2)  / 1 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "70121-1711-2", "marketing_start_date": "20240108"}, {"sample": false, "description": "24 POUCH in 1 CARTON (70121-1711-9)  / 1 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "70121-1711-9", "marketing_start_date": "20230519"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "70121-1711_4751c8c4-1971-44bb-8311-fea390cc1b98", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "70121-1711", "generic_name": "Dexmedetomidine Hydrochloride in Sodium Chloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine Hydrochloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA216604", "marketing_category": "ANDA", "marketing_start_date": "20230519", "listing_expiration_date": "20261231"}