etomidate

Generic: etomidate

Labeler: civica, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name etomidate
Generic Name etomidate
Labeler civica, inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

etomidate 2 mg/mL

Manufacturer
Civica, Inc.

Identifiers & Regulatory

Product NDC 72572-161
Product ID 72572-161_380f0c88-03f8-4cfa-8823-4766c2f7700c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202354
Listing Expiration 2026-12-31
Marketing Start 2022-03-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572161
Hyphenated Format 72572-161

Supplemental Identifiers

RxCUI
1654006 1654008
UNII
Z22628B598
NUI
N0000175975 N0000175681

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (72572-161-10) / 20 mL in 1 VIAL, SINGLE-DOSE (72572-161-01)
source: ndc

Packages (1)

72572-161-10 10 VIAL, SINGLE-DOSE in 1 CARTON (72572-161-10) / 20 mL in 1 VIAL, SINGLE-DOSE (72572-161-01)

Ingredients (1)

etomidate (2 mg/mL)

Linked Drug Pages (1)

Etomidate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "380f0c88-03f8-4cfa-8823-4766c2f7700c", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654006", "1654008"], "spl_set_id": ["98002094-f065-4b5f-963f-2c34b5241316"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72572-161-10)  / 20 mL in 1 VIAL, SINGLE-DOSE (72572-161-01)", "package_ndc": "72572-161-10", "marketing_start_date": "20220301"}], "brand_name": "Etomidate", "product_id": "72572-161_380f0c88-03f8-4cfa-8823-4766c2f7700c", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "72572-161", "generic_name": "Etomidate", "labeler_name": "Civica, Inc.", "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": "20220301", "listing_expiration_date": "20261231"}