Drugplain

NUEDEXTA 20 mg/1

dextromethorphan hydrobromide and quinidine sulfate · CAPSULE, GELATIN COATED · Avanir Pharmaceuticals, Inc.

No Recall History
Plain English

NUEDEXTA is a capsule, gelatin coated containing dextromethorphan hydrobromide and quinidine sulfate at 20 mg/1, taken oral. Manufactured by Avanir Pharmaceuticals, Inc..

Key Facts

Brand Name
NUEDEXTA
Generic Name
dextromethorphan hydrobromide and quinidine sulfate
NDC Code (Product)
64597-301
Manufacturer
Avanir Pharmaceuticals, Inc.
Strength
20 mg/1
Dosage Form
CAPSULE, GELATIN COATED
Route
ORAL
Marketing Status
Application #
NDA021879
Marketing Start
12/01/2010

Recall History

No Recall History

Frequently Asked Questions

What is NUEDEXTA used for?

NUEDEXTA contains dextromethorphan hydrobromide and quinidine sulfate. It is a capsule, gelatin coated taken oral. Consult your doctor for specific uses.

Is NUEDEXTA a controlled substance?

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

What is the generic name for NUEDEXTA?

The generic name for NUEDEXTA is dextromethorphan hydrobromide and quinidine sulfate. There are 2 other brand versions of dextromethorphan hydrobromide and quinidine sulfate.

What is the NDC code for NUEDEXTA 20 mg/1?

The NDC (National Drug Code) for NUEDEXTA 20 mg/1 is 64597-301, listed by Avanir Pharmaceuticals, Inc..

Product NDC

64597-301

Package NDC

64597-301-13

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

Data from openFDA · Public domain (CC0 1.0)