Latuda
lurasidone hydrochloride
- Strength
- 120 mg/1
- Form
- Tablet, Film Coated
- Class
- Atypical Antipsychotic
Sumitomo Pharma America, Inc.
Listed by MAJOR PHARMACEUTICALS
| Dosage form | Tablet, Film Coated |
|---|---|
| Route | Oral |
| Drug class | Atypical Antipsychotic |
| Approval route | ANDA — approved generic |
| NDC code | 0904-7421 |
| FDA application | ANDA208037 |
| RxNorm concept | 1040031 |
| Package sizes listed | 1 |
| Marketed since | February 2023 |
Same active ingredient, different manufacturer, strength or form. Products matching on both ingredient and strength are usually interchangeable — but confirm before switching, especially with modified-release forms.
lurasidone hydrochloride
Sumitomo Pharma America, Inc.
lurasidone hydrochloride
Sumitomo Pharma America, Inc.
lurasidone hydrochloride
Sumitomo Pharma America, Inc.
lurasidone hydrochloride
Sumitomo Pharma America, Inc.
lurasidone hydrochloride
Sumitomo Pharma America, Inc.
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Information only, not medical advice. Nothing on this page indicates that a medication is safe or suitable for you. Speak to a prescriber or pharmacist before starting, stopping or switching any medicine.
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