Amidate

Product NDC

0409-8060

11-digit product format

004098060

Labeler code

0409

Product ID

0409-8060_a340b83a-31e1-4e42-800b-3f8de5975f86

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Etomidate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA018227

Marketing category

NDA

Marketing start

2005-10-07

Marketing end

0000-00-00

Substance

ETOMIDATE

Active strength

2 mg/mL

Pharmacologic classes

General Anesthesia [PE],General Anesthetic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record