Lurasidone hydrochloride 20 mg/1
Lurasidone hydrochloride · TABLET, COATED · Zydus Pharmaceuticals USA Inc.
Lurasidone hydrochloride is a tablet, coated containing lurasidone hydrochloride at 20 mg/1, taken oral. Manufactured by Zydus Pharmaceuticals USA Inc..
Key Facts
- Brand Name
- Lurasidone hydrochloride
- Generic Name
- Lurasidone hydrochloride
- NDC Code (Product)
68382-965- Manufacturer
- Zydus Pharmaceuticals USA Inc.
- Strength
- 20 mg/1
- Dosage Form
- TABLET, COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA208052
- Marketing Start
- 02/01/2023
Recall History
No Recall HistoryFrequently Asked Questions
What is Lurasidone hydrochloride used for?
Lurasidone hydrochloride contains Lurasidone hydrochloride. It is a tablet, coated taken oral. Consult your doctor for specific uses.
Is Lurasidone hydrochloride a controlled substance?
Lurasidone hydrochloride is not classified as a controlled substance by the DEA.
What is the generic name for Lurasidone hydrochloride?
The generic name for Lurasidone hydrochloride is Lurasidone hydrochloride. There are 12 other brand versions of Lurasidone hydrochloride.
What is the NDC code for Lurasidone hydrochloride 20 mg/1?
The NDC (National Drug Code) for Lurasidone hydrochloride 20 mg/1 is 68382-965, listed by Zydus Pharmaceuticals USA Inc..
Other Lurasidone Brands
See all →- Lurasidone Hydrochloride80 mg/113668-466
- Lurasidone Hydrochloride60 mg/153746-082
- Lurasidone Hydrochloride80 mg/153746-881
- Lurasidone Hydrochloride20 mg/160687-747
- Lurasidone Hydrochloride60 mg/162332-496
- Latuda40 mg/163402-304
- LURASIDONE HYDROCHLORIDE20 mg/165862-953
- lurasidone hydrochloride20 mg/168180-670
- lurasidone hydrochloride80 mg/168180-673
- Lurasidone Hydrochloride20 mg/170518-4563
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)