etomidate injection, solution (51662-1634)

Drug Facts

Product Profile

Brand Name etomidate injection, solution

Generic Name etomidate injection, solution

Labeler hf acquisition co llc, dba healthfirst

Dosage Form INJECTION, SOLUTION

Routes

INTRAVENOUS

Active Ingredients

etomidate 20 mg/10mL

Manufacturer

HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1634

Product ID 51662-1634_0635683b-880b-0cd4-e063-6394a90ab73e

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA206126

Listing Expiration 2026-12-31

Marketing Start 2023-09-25

Pharmacologic Class

Established (EPC)

general anesthetic [epc]

Physiologic Effect

general anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621634

Hyphenated Format 51662-1634

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 etomidate injection, solution (source: ndc)

Generic Name etomidate injection, solution (source: ndc)

Application Number ANDA206126 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

20 mg/10mL

source: ndc

Packaging

10 mL in 1 VIAL, SINGLE-DOSE (51662-1634-1)

source: ndc

Packages (1)

51662-1634-1 10 mL in 1 VIAL, SINGLE-DOSE (51662-1634-1)

Ingredients (1)

etomidate (20 mg/10mL)

Linked Drug Pages (1)

ETOMIDATE injection, solution ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "0635683b-880b-0cd4-e063-6394a90ab73e", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654006"], "spl_set_id": ["0635683b-880a-0cd4-e063-6394a90ab73e"], "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 (51662-1634-1)", "package_ndc": "51662-1634-1", "marketing_start_date": "20230925"}], "brand_name": "ETOMIDATE injection, solution", "product_id": "51662-1634_0635683b-880b-0cd4-e063-6394a90ab73e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1634", "generic_name": "ETOMIDATE injection, solution", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETOMIDATE injection, solution", "active_ingredients": [{"name": "ETOMIDATE", "strength": "20 mg/10mL"}], "application_number": "ANDA206126", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}