etomidate
Generic: etomidate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
etomidate
Generic Name
etomidate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
etomidate 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1485
Product ID
51662-1485_2b39a9d5-ca76-b107-e063-6394a90ae8bb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202354
Listing Expiration
2026-12-31
Marketing Start
2020-01-11
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621485
Hyphenated Format
51662-1485
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA202354 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 10 mL in 1 VIAL, SINGLE-DOSE (51662-1485-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2b39a9d5-ca76-b107-e063-6394a90ae8bb", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654006"], "spl_set_id": ["9bdee875-4b48-c592-e053-2995a90a6485"], "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": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1485-1)", "package_ndc": "51662-1485-1", "marketing_start_date": "20200111"}], "brand_name": "ETOMIDATE", "product_id": "51662-1485_2b39a9d5-ca76-b107-e063-6394a90ae8bb", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1485", "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": "2 mg/mL"}], "application_number": "ANDA202354", "marketing_category": "ANDA", "marketing_start_date": "20200111", "listing_expiration_date": "20261231"}