Drugplain

NEUROLITE

Bicisate dihydrochloride · KIT · Lantheus Medical Imaging, Inc.

No Recall History
Plain English

NEUROLITE is a kit containing bicisate dihydrochloride. Manufactured by Lantheus Medical Imaging, Inc..

Key Facts

Brand Name
NEUROLITE
Generic Name
Bicisate dihydrochloride
NDC Code (Product)
11994-006
Manufacturer
Lantheus Medical Imaging, Inc.
Dosage Form
KIT
Marketing Status
Application #
NDA020256
Marketing Start
11/23/1994

Recall History

No Recall History

Frequently Asked Questions

What is NEUROLITE used for?

NEUROLITE contains Bicisate dihydrochloride. It is a kit taken as directed. Consult your doctor for specific uses.

Is NEUROLITE a controlled substance?

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

What is the generic name for NEUROLITE?

The generic name for NEUROLITE is Bicisate dihydrochloride. There are no other listed brand versions of Bicisate dihydrochloride.

What is the NDC code for NEUROLITE ?

The NDC (National Drug Code) for NEUROLITE is 11994-006, listed by Lantheus Medical Imaging, Inc..

Product NDC

11994-006

Package NDC

11994-006-02

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

Data from openFDA · Public domain (CC0 1.0)