Package 51662-1371-1

Brand: esmolol hydrochloride

Generic: esmolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1371-1
Digits Only 5166213711
Product NDC 51662-1371
Product ID 51662-1371_ef7bd5a0-02aa-7b66-e053-2995a90a8ffa
Description

10 mL in 1 VIAL, SINGLE-DOSE (51662-1371-1)

Marketing

Marketing Status
Marketed Since 2019-12-08
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": "ef7bd5a0-02aa-7b66-e053-2995a90a8ffa", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["993df35b-0006-4892-e053-2a95a90a0dba"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1371-1)", "package_ndc": "51662-1371-1", "marketing_start_date": "20191208"}], "brand_name": "ESMOLOL HYDROCHLORIDE", "product_id": "51662-1371_ef7bd5a0-02aa-7b66-e053-2995a90a8ffa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1371", "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": "ANDA076573", "marketing_category": "ANDA", "marketing_start_date": "20191208", "listing_expiration_date": "20261231"}