etomidate

Generic: etomidate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name etomidate
Generic Name etomidate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

etomidate 40 mg/20mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1542
Product ID 51662-1542_dc43b289-4f33-1c1e-e053-2995a90a3a23
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206126
Listing Expiration 2026-12-31
Marketing Start 2022-04-09

Pharmacologic Class

Established (EPC)
general anesthetic [epc]
Physiologic Effect
general anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621542
Hyphenated Format 51662-1542

Supplemental Identifiers

RxCUI
1654008
UNII
Z22628B598
NUI
N0000175975 N0000175681

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 etomidate (source: ndc)
Generic Name etomidate (source: ndc)
Application Number ANDA206126 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/20mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)
source: ndc

Packages (1)

51662-1542-1 20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)

Ingredients (1)

etomidate (40 mg/20mL)

Linked Drug Pages (1)

ETOMIDATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "dc43b289-4f33-1c1e-e053-2995a90a3a23", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654008"], "spl_set_id": ["dc43b289-4f32-1c1e-e053-2995a90a3a23"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)", "package_ndc": "51662-1542-1", "marketing_start_date": "20220409"}], "brand_name": "ETOMIDATE", "product_id": "51662-1542_dc43b289-4f33-1c1e-e053-2995a90a3a23", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1542", "generic_name": "ETOMIDATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETOMIDATE", "active_ingredients": [{"name": "ETOMIDATE", "strength": "40 mg/20mL"}], "application_number": "ANDA206126", "marketing_category": "ANDA", "marketing_start_date": "20220409", "listing_expiration_date": "20261231"}