amidate(tm) etomidate (51662-1459)

Drug Facts

Product Profile

Brand Name amidate(tm) etomidate

Generic Name amidate(tm) etomidate

Labeler hf acquisition co llc, dba healthfirst

Dosage Form INJECTION, SOLUTION

Routes

INTRAVENOUS

Active Ingredients

etomidate 2 mg/mL

Manufacturer

HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1459

Product ID 51662-1459_0762982e-561c-4595-e063-6394a90a58b3

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category NDA

Application Number NDA018227

Listing Expiration 2026-12-31

Marketing Start 2020-03-31

Pharmacologic Class

Established (EPC)

general anesthetic [epc]

Physiologic Effect

general anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621459

Hyphenated Format 51662-1459

Supplemental Identifiers

RxCUI

1654006

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 amidate(tm) etomidate (source: ndc)

Generic Name amidate(tm) etomidate (source: ndc)

Application Number NDA018227 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

2 mg/mL

source: ndc

Packaging

10 mL in 1 VIAL, SINGLE-USE (51662-1459-1)

source: ndc

Packages (1)

51662-1459-1 10 mL in 1 VIAL, SINGLE-USE (51662-1459-1)

Ingredients (1)

etomidate (2 mg/mL)

Linked Drug Pages (1)

AMIDATE(TM) ETOMIDATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "0762982e-561c-4595-e063-6394a90a58b3", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654006"], "spl_set_id": ["a227d2f1-3eef-4ac6-e053-2995a90a5340"], "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-USE (51662-1459-1)", "package_ndc": "51662-1459-1", "marketing_start_date": "20200331"}], "brand_name": "AMIDATE(TM) ETOMIDATE", "product_id": "51662-1459_0762982e-561c-4595-e063-6394a90a58b3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1459", "generic_name": "AMIDATE(TM) ETOMIDATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMIDATE(TM) ETOMIDATE", "active_ingredients": [{"name": "ETOMIDATE", "strength": "2 mg/mL"}], "application_number": "NDA018227", "marketing_category": "NDA", "marketing_start_date": "20200331", "listing_expiration_date": "20261231"}