etomidate
Generic: etomidate
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
etomidate
Generic Name
etomidate
Labeler
eugia us llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
etomidate 20 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
55150-221
Product ID
55150-221_278b160e-cdc4-451e-9405-cb001f443680
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206126
Listing Expiration
2026-12-31
Marketing Start
2017-02-24
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150221
Hyphenated Format
55150-221
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 (source: ndc)
Application Number
ANDA206126 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/10mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-221-10) / 10 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "278b160e-cdc4-451e-9405-cb001f443680", "openfda": {"nui": ["N0000175975", "N0000175681"], "upc": ["0355150221103"], "unii": ["Z22628B598"], "rxcui": ["1654006", "1654008"], "spl_set_id": ["0820f15a-046b-4185-a2b3-2e4051ee3d82"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (55150-221-10) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-221-10", "marketing_start_date": "20170224"}], "brand_name": "ETOMIDATE", "product_id": "55150-221_278b160e-cdc4-451e-9405-cb001f443680", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "55150-221", "generic_name": "ETOMIDATE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETOMIDATE", "active_ingredients": [{"name": "ETOMIDATE", "strength": "20 mg/10mL"}], "application_number": "ANDA206126", "marketing_category": "ANDA", "marketing_start_date": "20170224", "listing_expiration_date": "20261231"}