esmolol hydrochloride

Generic: esmolol hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name esmolol hydrochloride
Generic Name esmolol hydrochloride
Labeler remedyrepack inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

esmolol hydrochloride 100 mg/10mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4410
Product ID 70518-4410_3b14985c-f435-be98-e063-6294a90a0f92
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205520
Listing Expiration 2026-12-31
Marketing Start 2025-07-29

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184410
Hyphenated Format 70518-4410

Supplemental Identifiers

RxCUI
1736546
UNII
V05260LC8D

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name esmolol hydrochloride (source: ndc)
Generic Name esmolol hydrochloride (source: ndc)
Application Number ANDA205520 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/10mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4410-0) / 10 mL in 1 VIAL, SINGLE-DOSE (70518-4410-1)
source: ndc

Packages (1)

Ingredients (1)

esmolol hydrochloride (100 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3b14985c-f435-be98-e063-6294a90a0f92", "openfda": {"unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["1f5707f2-a8a7-4a5f-b846-64585b5e3f9f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4410-0)  / 10 mL in 1 VIAL, SINGLE-DOSE (70518-4410-1)", "package_ndc": "70518-4410-0", "marketing_start_date": "20250729"}], "brand_name": "Esmolol Hydrochloride", "product_id": "70518-4410_3b14985c-f435-be98-e063-6294a90a0f92", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4410", "generic_name": "Esmolol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20250729", "listing_expiration_date": "20261231"}