Package 14789-011-01

Brand: isoproterenol hydrochloride

Generic: isoproterenol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 14789-011-01
Digits Only 1478901101
Product NDC 14789-011
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (14789-011-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2017-08-03
Brand isoproterenol hydrochloride
Generic isoproterenol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3ef21b9c-b314-713e-e063-6394a90a9e86", "openfda": {"upc": ["0314789011011"], "unii": ["DIA2A74855"], "rxcui": ["1667909", "1667915"], "spl_set_id": ["dfb97590-dcbf-47e7-bbfe-f01580eb6ed0"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (14789-011-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "14789-011-01", "marketing_start_date": "20170803"}], "brand_name": "Isoproterenol Hydrochloride", "product_id": "14789-011_3ef21b9c-b314-713e-e063-6394a90a9e86", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "14789-011", "generic_name": "Isoproterenol Hydrochloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoproterenol Hydrochloride", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA206961", "marketing_category": "ANDA", "marketing_start_date": "20170803", "listing_expiration_date": "20261231"}