Package 51662-1444-1

{"route": ["INTRAVENOUS"], "spl_id": "101e0203-54eb-a48a-e063-6294a90af0d0", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["9a52d2fd-e551-f8f1-e053-2995a90a6c09"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1444-1)", "package_ndc": "51662-1444-1", "marketing_start_date": "20191222"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1444-3)  / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1444-2)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1444-3", "marketing_start_date": "20220912"}], "brand_name": "ESMOLOL HYDROCHLORIDE", "product_id": "51662-1444_101e0203-54eb-a48a-e063-6294a90af0d0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1444", "generic_name": "ESMOLOL HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESMOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "ESMOLOL HYDROCHLORIDE", "strength": "100 mg/10mL"}], "application_number": "ANDA205520", "marketing_category": "ANDA", "marketing_start_date": "20191222", "listing_expiration_date": "20261231"}