esmolol hydrochloride
Generic: esmolol hydrochloride
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
esmolol hydrochloride
Generic Name
esmolol hydrochloride
Labeler
baxter healthcare corporation
Dosage Form
INJECTION
Routes
Active Ingredients
esmolol hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
10019-120
Product ID
10019-120_8f3d3389-00ba-4863-b73b-74d2e49c34c2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019386
Listing Expiration
2026-12-31
Marketing Start
1986-12-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10019120
Hyphenated Format
10019-120
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
NDA019386 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL in 1 CARTON (10019-120-01) / 10 mL in 1 VIAL (10019-120-39)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "8f3d3389-00ba-4863-b73b-74d2e49c34c2", "openfda": {"upc": ["0310019120010"], "unii": ["V05260LC8D"], "rxcui": ["1736546"], "spl_set_id": ["f0a56c07-8f0f-4499-8d00-f13a966bf988"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (10019-120-01) / 10 mL in 1 VIAL (10019-120-39)", "package_ndc": "10019-120-01", "marketing_start_date": "19861231"}], "brand_name": "Esmolol Hydrochloride", "product_id": "10019-120_8f3d3389-00ba-4863-b73b-74d2e49c34c2", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "10019-120", "generic_name": "Esmolol Hydrochloride", "labeler_name": "Baxter Healthcare Corporation", "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"}