Drugplain

Lucemyra .2 mg/1

lofexidine hydrochloride · TABLET, FILM COATED · USWM, LLC

No Recall History
Plain English

Lucemyra is a tablet, film coated containing lofexidine hydrochloride at .2 mg/1, taken oral. Manufactured by USWM, LLC.

Key Facts

Brand Name
Lucemyra
Generic Name
lofexidine hydrochloride
NDC Code (Product)
78670-050
Manufacturer
USWM, LLC
Strength
.2 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA209229
Marketing Start
02/09/2021

Recall History

No Recall History

Frequently Asked Questions

What is Lucemyra used for?

Lucemyra contains lofexidine hydrochloride. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Lucemyra a controlled substance?

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

What is the generic name for Lucemyra?

The generic name for Lucemyra is lofexidine hydrochloride. There are 2 other brand versions of lofexidine hydrochloride.

What is the NDC code for Lucemyra .2 mg/1?

The NDC (National Drug Code) for Lucemyra .2 mg/1 is 78670-050, listed by USWM, LLC.

Product NDC

78670-050

Package NDC

78670-050-03

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

Data from openFDA · Public domain (CC0 1.0)