Package 67457-657-25

Brand: esmolol hydrochloride in sodium chloride

Generic: esmolol hydrochloride in sodium chloride
NDC Package

Package Facts

Identity

Package NDC 67457-657-25
Digits Only 6745765725
Product NDC 67457-657
Description

1 BAG in 1 POUCH (67457-657-25) / 250 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2018-09-04
Brand esmolol hydrochloride in sodium chloride
Generic esmolol hydrochloride in sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f5590283-06f2-43c7-9e1b-2a762f568bbf", "openfda": {"upc": ["0367457658100"], "unii": ["V05260LC8D"], "rxcui": ["979432", "1736541"], "spl_set_id": ["01ad7942-99c3-40ee-9cfb-272fb6c44e2b"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 POUCH (67457-657-25)  / 250 mL in 1 BAG", "package_ndc": "67457-657-25", "marketing_start_date": "20180904"}], "brand_name": "esmolol hydrochloride in sodium chloride", "product_id": "67457-657_f5590283-06f2-43c7-9e1b-2a762f568bbf", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67457-657", "generic_name": "esmolol hydrochloride in sodium chloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "esmolol hydrochloride in sodium chloride", "active_ingredients": [{"name": "ESMOLOL HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA206608", "marketing_category": "ANDA", "marketing_start_date": "20180904", "listing_expiration_date": "20261231"}