Drugplain

Precedex 4 ug/mL

DEXMEDETOMIDINE HYDROCHLORIDE · INJECTION, SOLUTION · Hospira, Inc.

No Recall HistoryCurrently in Shortage
Plain English

Precedex is a injection, solution containing dexmedetomidine hydrochloride at 4 ug/mL, taken intravenous. Manufactured by Hospira, Inc..

Key Facts

Brand Name
Precedex
Generic Name
DEXMEDETOMIDINE HYDROCHLORIDE
NDC Code (Product)
0409-1434
Manufacturer
Hospira, Inc.
Strength
4 ug/mL
Dosage Form
INJECTION, SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
NDA021038
Marketing Start
09/28/2020

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

bradycardia247 reports
off label use233 reports
hypotension171 reports
cardiac arrest168 reports
pyrexia111 reports
drug ineffective98 reports
pneumonia97 reports
product use in unapproved indication91 reports
product use issue89 reports
respiratory failure86 reports

Frequently Asked Questions

What is Precedex used for?

Precedex contains DEXMEDETOMIDINE HYDROCHLORIDE. It is a injection, solution taken intravenous. Consult your doctor for specific uses.

Is Precedex a controlled substance?

Precedex is not classified as a controlled substance by the DEA.

What is the generic name for Precedex?

The generic name for Precedex is DEXMEDETOMIDINE HYDROCHLORIDE. There are 10 other brand versions of DEXMEDETOMIDINE HYDROCHLORIDE.

What is the NDC code for Precedex 4 ug/mL?

The NDC (National Drug Code) for Precedex 4 ug/mL is 0409-1434, listed by Hospira, Inc..