Package 51662-1322-1

Brand: esmolol hydrochloride

Generic: esmolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1322-1
Digits Only 5166213221
Product NDC 51662-1322
Product ID 51662-1322_11c184fc-7404-be32-e063-6394a90aac35
Description

10 mL in 1 VIAL (51662-1322-1)

Marketing

Marketing Status
Marketed Since 2018-10-19
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": "11c184fc-7404-be32-e063-6394a90aac35", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["789730fa-eaca-4986-e053-2a91aa0a5339"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL (51662-1322-1)", "package_ndc": "51662-1322-1", "marketing_start_date": "20181019"}], "brand_name": "ESMOLOL HYDROCHLORIDE", "product_id": "51662-1322_11c184fc-7404-be32-e063-6394a90aac35", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1322", "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": "ANDA076474", "marketing_category": "ANDA", "marketing_start_date": "20181019", "listing_expiration_date": "20261231"}