Nuedexta 20 mg/1
dextromethorphan hydrobromide and quinidine sulfate · CAPSULE, GELATIN COATED · Otsuka America Pharmaceutical, Inc
Nuedexta is a capsule, gelatin coated containing dextromethorphan hydrobromide and quinidine sulfate at 20 mg/1, taken oral. Manufactured by Otsuka America Pharmaceutical, Inc.
Key Facts
- Brand Name
- Nuedexta
- Generic Name
- dextromethorphan hydrobromide and quinidine sulfate
- NDC Code (Product)
59148-053- Manufacturer
- Otsuka America Pharmaceutical, Inc
- Strength
- 20 mg/1
- Dosage Form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA021879
- Marketing Start
- 01/03/2023
Recall History
No Recall HistoryFrequently 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 59148-053, listed by Otsuka America Pharmaceutical, Inc.