Package 67457-182-10

Brand: esmolol hydrochloride

Generic: esmolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-182-10
Digits Only 6745718210
Product NDC 67457-182
Description

10 VIAL in 1 CARTON (67457-182-10) / 10 mL in 1 VIAL (67457-182-00)

Marketing

Marketing Status
Marketed Since 2007-05-29
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": "677a4e72-7b0a-4f6c-b82e-091d93588566", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["94f069f9-dd52-4a69-a103-ebdb4294f088"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (67457-182-10)  / 10 mL in 1 VIAL (67457-182-00)", "package_ndc": "67457-182-10", "marketing_start_date": "20070529"}], "brand_name": "Esmolol Hydrochloride", "product_id": "67457-182_677a4e72-7b0a-4f6c-b82e-091d93588566", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67457-182", "generic_name": "esmolol hydrochloride", "labeler_name": "Mylan Institutional LLC", "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": "20070529", "listing_expiration_date": "20261231"}