etomidate
Generic: etomidate injection
Labeler: fosun pharma usa incDrug Facts
Product Profile
Brand Name
etomidate
Generic Name
etomidate injection
Labeler
fosun pharma usa inc
Dosage Form
SOLUTION
Routes
Active Ingredients
etomidate 2 mg/mL
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72266147
Hyphenated Format
72266-147
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 10 VIAL in 1 CARTON (72266-147-10) / 20 mL in 1 VIAL (72266-147-01)
Packages (1)
Ingredients (1)
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"}