Etomidate

Product NDC

23155-522

11-digit product format

231550522

Labeler code

23155

Product ID

23155-522_151cc356-7566-4258-b675-a8219ddb5f29

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Etomidate

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

Heritage Pharmaceuticals Inc.

Application

ANDA204618

Marketing category

ANDA

Marketing start

2012-09-13

Marketing end

0000-00-00

Substance

ETOMIDATE

Active strength

2 mg/mL

Pharmacologic classes

General Anesthesia [PE],General Anesthetic [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record