Etomidate

Product NDC

70518-1003

11-digit product format

705181003

Labeler code

70518

Product ID

70518-1003_6491f76a-592f-639f-e053-2991aa0a1196

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

etomidate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

ANDA209058

Marketing category

ANDA

Marketing start

2018-02-06

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

2019-12-31

Current FDA listing

Historical FDA.report record