Package 51662-1427-1

Brand: esmolol hydrochloride

Generic: esmolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1427-1
Digits Only 5166214271
Product NDC 51662-1427
Product ID 51662-1427_2b3832b9-14ba-a453-e063-6394a90a0330
Description

250 mL in 1 BAG (51662-1427-1)

Marketing

Marketing Status
Marketed Since 2019-12-21
Brand esmolol hydrochloride
Generic esmolol hydrochloride
Sample Package No

Linked Drug Pages (1)

ESMOLOL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2b3832b9-14ba-a453-e063-6394a90a0330", "openfda": {"upc": ["0310019055619"], "unii": ["V05260LC8D"], "rxcui": ["1736541"], "spl_set_id": ["9a3e69ab-3ffe-33af-e053-2a95a90a6524"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1427-1)", "package_ndc": "51662-1427-1", "marketing_start_date": "20191221"}], "brand_name": "ESMOLOL HYDROCHLORIDE", "product_id": "51662-1427_2b3832b9-14ba-a453-e063-6394a90a0330", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1427", "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": "10 mg/mL"}], "application_number": "NDA019386", "marketing_category": "NDA", "marketing_start_date": "20191221", "listing_expiration_date": "20261231"}