esmolol hydrochloride in sodium chloride
Generic: esmolol hydrochloride in sodium chloride
Labeler: mylan institutional llcDrug Facts
Product Profile
Brand Name
esmolol hydrochloride in sodium chloride
Generic Name
esmolol hydrochloride in sodium chloride
Labeler
mylan institutional llc
Dosage Form
INJECTION
Routes
Active Ingredients
esmolol hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
67457-657
Product ID
67457-657_f5590283-06f2-43c7-9e1b-2a762f568bbf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206608
Listing Expiration
2026-12-31
Marketing Start
2018-09-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67457657
Hyphenated Format
67457-657
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 in sodium chloride (source: ndc)
Generic Name
esmolol hydrochloride in sodium chloride (source: ndc)
Application Number
ANDA206608 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 BAG in 1 POUCH (67457-657-25) / 250 mL in 1 BAG
Packages (1)
Ingredients (1)
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"}