Drugplain

AMIDATE(TM) ETOMIDATE 2 mg/mL

AMIDATE(TM) ETOMIDATE · INJECTION, SOLUTION · HF Acquisition Co LLC, DBA HealthFirst

No Recall History
Plain English

AMIDATE(TM) ETOMIDATE is a injection, solution containing amidate(tm) etomidate at 2 mg/mL, taken intravenous. Manufactured by HF Acquisition Co LLC, DBA HealthFirst.

Key Facts

Brand Name
AMIDATE(TM) ETOMIDATE
Generic Name
AMIDATE(TM) ETOMIDATE
NDC Code (Product)
51662-1459
Manufacturer
HF Acquisition Co LLC, DBA HealthFirst
Strength
2 mg/mL
Dosage Form
INJECTION, SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
NDA018227
Drug Class
General Anesthetic [EPC]
Marketing Start
03/31/2020

Recall History

No Recall History

Frequently Asked Questions

What is AMIDATE(TM) ETOMIDATE used for?

AMIDATE(TM) ETOMIDATE contains AMIDATE(TM) ETOMIDATE. It is a injection, solution taken intravenous. Consult your doctor for specific uses.

Is AMIDATE(TM) ETOMIDATE a controlled substance?

AMIDATE(TM) ETOMIDATE is not classified as a controlled substance by the DEA.

What is the generic name for AMIDATE(TM) ETOMIDATE?

The generic name for AMIDATE(TM) ETOMIDATE is AMIDATE(TM) ETOMIDATE. There are no other listed brand versions of AMIDATE(TM) ETOMIDATE.

What is the NDC code for AMIDATE(TM) ETOMIDATE 2 mg/mL?

The NDC (National Drug Code) for AMIDATE(TM) ETOMIDATE 2 mg/mL is 51662-1459, listed by HF Acquisition Co LLC, DBA HealthFirst.

Product NDC

51662-1459

Package NDC

51662-1459-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)