Package 84549-194-10
Brand: esmolol hydrochloride
Generic: esmolol hydrochloridePackage Facts
Identity
Package NDC
84549-194-10
Digits Only
8454919410
Product NDC
84549-194
Description
10 mL in 1 VIAL, SINGLE-DOSE (84549-194-10)
Marketing
Marketing Status
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": "463cc756-d1d0-9ffe-e063-6394a90ab342", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["3853a26d-782d-f4e7-e063-6294a90a6e47"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (84549-194-10)", "package_ndc": "84549-194-10", "marketing_start_date": "20250827"}], "brand_name": "Esmolol Hydrochloride", "product_id": "84549-194_463cc756-d1d0-9ffe-e063-6394a90ab342", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "84549-194", "generic_name": "Esmolol Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Esmolol Hydrochloride", "active_ingredients": [{"name": "ESMOLOL HYDROCHLORIDE", "strength": "100 mg/10mL"}], "application_number": "ANDA205520", "marketing_category": "ANDA", "marketing_start_date": "20150723", "listing_expiration_date": "20261231"}