Package 71872-7136-1

Brand: esmolol hydrochloride

Generic: esmolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7136-1
Digits Only 7187271361
Product NDC 71872-7136
Description

1 VIAL in 1 BAG (71872-7136-1) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-04-19
Brand esmolol hydrochloride
Generic esmolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fc4a1996-71bf-fff1-e053-6394a90a2de0", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["6bdd5315-75ce-1537-e053-2991aa0a6549"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7136-1)  / 10 mL in 1 VIAL", "package_ndc": "71872-7136-1", "marketing_start_date": "20180419"}], "brand_name": "Esmolol Hydrochloride", "product_id": "71872-7136_fc4a1996-71bf-fff1-e053-6394a90a2de0", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71872-7136", "generic_name": "Esmolol Hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "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": "19861231", "listing_expiration_date": "20261231"}