etomidate

Generic: etomidate injection

Labeler: fosun pharma usa inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name etomidate
Generic Name etomidate injection
Labeler fosun pharma usa inc
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

etomidate 2 mg/mL

Manufacturer
Fosun Pharma USA Inc

Identifiers & Regulatory

Product NDC 72266-147
Product ID 72266-147_2b365133-b609-3285-e063-6394a90a69a6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209058
Listing Expiration 2026-12-31
Marketing Start 2019-09-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266147
Hyphenated Format 72266-147

Supplemental Identifiers

RxCUI
1654006 1654008
UPC
0372266147103 0372266147011 0372266146106
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 injection (source: ndc)
Application Number ANDA209058 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (72266-147-10) / 20 mL in 1 VIAL (72266-147-01)
source: ndc

Packages (1)

Ingredients (1)

etomidate (2 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2b365133-b609-3285-e063-6394a90a69a6", "openfda": {"nui": ["N0000175975", "N0000175681"], "upc": ["0372266147103", "0372266147011", "0372266146106"], "unii": ["Z22628B598"], "rxcui": ["1654006", "1654008"], "spl_set_id": ["8b6c54d8-3f3f-4290-841c-976bea01086f"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Fosun Pharma USA Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72266-147-10)  / 20 mL in 1 VIAL (72266-147-01)", "package_ndc": "72266-147-10", "marketing_start_date": "20190903"}], "brand_name": "Etomidate", "product_id": "72266-147_2b365133-b609-3285-e063-6394a90a69a6", "dosage_form": "SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "72266-147", "generic_name": "Etomidate Injection", "labeler_name": "Fosun Pharma USA Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Etomidate", "active_ingredients": [{"name": "ETOMIDATE", "strength": "2 mg/mL"}], "application_number": "ANDA209058", "marketing_category": "ANDA", "marketing_start_date": "20190903", "listing_expiration_date": "20261231"}