DEA schedule
Is lurasidone a controlled substance?
Federal schedule for lurasidone from the FDA NDC directory, checked against the DEA controlled substances list.
Source: FDA NDC Directory file dated 2026-10-22. Publisher page
No. Lurasidone is not a federally controlled substance. None of its FDA NDC listings carries a DEA schedule, and lurasidone is not on the DEA controlled substances list.
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Schedule check
| Source | What it lists |
|---|---|
| FDA NDC directory | 136 prescription listings from 30 labelers, none with a DEA schedule |
| DEA controlled substances list | lurasidone is not on the list |
Lurasidone NDC listings
| NDC | Product | Form | Strength | Labeler | DEA schedule |
|---|---|---|---|---|---|
| 63402-312 | Latuda | tablet, film coated | 120 mg/1 | Sumitomo Pharma America, Inc. | None |
| 63402-302 | Latuda | tablet, film coated | 20 mg/1 | Sumitomo Pharma America, Inc. | None |
| 63402-304 | Latuda | tablet, film coated | 40 mg/1 | Sumitomo Pharma America, Inc. | None |
| 63402-306 | Latuda | tablet, film coated | 60 mg/1 | Sumitomo Pharma America, Inc. | None |
| 63402-308 | Latuda | tablet, film coated | 80 mg/1 | Sumitomo Pharma America, Inc. | None |
| 72189-598 | Lurasidone HCL | tablet | 40 mg/1 | Direct_rx | None |
| 47335-579 | Lurasidone Hydrochloride | tablet | 120 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 65862-957 | LURASIDONE HYDROCHLORIDE | tablet | 120 mg/1 | Aurobindo Pharma Limited | None |
| 68180-674 | lurasidone hydrochloride | tablet | 120 mg/1 | Lupin Pharmaceuticals, Inc. | None |
| 47335-578 | Lurasidone Hydrochloride | tablet | 20 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 65862-953 | LURASIDONE HYDROCHLORIDE | tablet | 20 mg/1 | Aurobindo Pharma Limited | None |
| 68180-670 | lurasidone hydrochloride | tablet | 20 mg/1 | Lupin Pharmaceuticals, Inc. | None |
| 82804-215 | LURASIDONE HYDROCHLORIDE | tablet | 20 mg/1 | Proficient Rx LP | None |
| 47335-684 | Lurasidone Hydrochloride | tablet | 40 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 65862-954 | LURASIDONE HYDROCHLORIDE | tablet | 40 mg/1 | Aurobindo Pharma Limited | None |
| 68180-671 | lurasidone hydrochloride | tablet | 40 mg/1 | Lupin Pharmaceuticals, Inc. | None |
| 70518-4427 | lurasidone hydrochloride | tablet | 40 mg/1 | REMEDYREPACK INC. | None |
| 47335-639 | Lurasidone Hydrochloride | tablet | 60 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 65862-955 | LURASIDONE HYDROCHLORIDE | tablet | 60 mg/1 | Aurobindo Pharma Limited | None |
| 67046-1654 | LURASIDONE HYDROCHLORIDE | tablet | 60 mg/1 | Coupler LLC | None |
| 68180-672 | lurasidone hydrochloride | tablet | 60 mg/1 | Lupin Pharmaceuticals, Inc. | None |
| 47335-685 | Lurasidone Hydrochloride | tablet | 80 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 65862-956 | LURASIDONE HYDROCHLORIDE | tablet | 80 mg/1 | Aurobindo Pharma Limited | None |
| 68180-673 | lurasidone hydrochloride | tablet | 80 mg/1 | Lupin Pharmaceuticals, Inc. | None |
| 53746-882 | Lurasidone Hydrochloride | tablet, coated | 120 mg/1 | Amneal Pharmaceuticals of New York LLC | None |
| 65162-882 | Lurasidone Hydrochloride | tablet, coated | 120 mg/1 | Amneal Pharmaceuticals LLC | None |
| 68382-968 | Lurasidone hydrochloride | tablet, coated | 120 mg/1 | Zydus Pharmaceuticals USA Inc. | None |
| 70771-1738 | Lurasidone hydrochloride | tablet, coated | 120 mg/1 | Zydus Lifesciences Limited | None |
| 53746-879 | Lurasidone Hydrochloride | tablet, coated | 20 mg/1 | Amneal Pharmaceuticals of New York LLC | None |
| 65162-879 | Lurasidone Hydrochloride | tablet, coated | 20 mg/1 | Amneal Pharmaceuticals LLC | None |
| 68382-965 | Lurasidone hydrochloride | tablet, coated | 20 mg/1 | Zydus Pharmaceuticals USA Inc. | None |
| 70771-1734 | Lurasidone hydrochloride | tablet, coated | 20 mg/1 | Zydus Lifesciences Limited | None |
| 53746-880 | Lurasidone Hydrochloride | tablet, coated | 40 mg/1 | Amneal Pharmaceuticals of New York LLC | None |
| 65162-880 | Lurasidone Hydrochloride | tablet, coated | 40 mg/1 | Amneal Pharmaceuticals LLC | None |
| 68382-966 | Lurasidone hydrochloride | tablet, coated | 40 mg/1 | Zydus Pharmaceuticals USA Inc. | None |
| 70771-1735 | Lurasidone hydrochloride | tablet, coated | 40 mg/1 | Zydus Lifesciences Limited | None |
| 53746-082 | Lurasidone Hydrochloride | tablet, coated | 60 mg/1 | Amneal Pharmaceuticals of New York LLC | None |
| 65162-082 | Lurasidone Hydrochloride | tablet, coated | 60 mg/1 | Amneal Pharmaceuticals LLC | None |
| 68382-859 | Lurasidone hydrochloride | tablet, coated | 60 mg/1 | Zydus Pharmaceuticals USA Inc. | None |
| 70771-1736 | Lurasidone hydrochloride | tablet, coated | 60 mg/1 | Zydus Lifesciences Limited | None |
Showing 40 of 136 listings.
Questions
Is lurasidone a controlled substance?
No. Lurasidone is not a federally controlled substance. None of its FDA NDC listings carries a DEA schedule, and lurasidone is not on the DEA controlled substances list.
Is lurasidone a narcotic?
No. Lurasidone is not on the DEA controlled substances list, so the DEA does not classify it as a narcotic. Its FDA established pharmacologic class is Atypical Antipsychotic.
Does this page cover state schedules?
No. This page reports the federal schedule only. Some states schedule drugs on their own; check your state board of pharmacy.
More on Lurasidone
- What is Lurasidone used for?FDA label uses
- Generic for LatudaFDA Orange Book
- What is Latuda used for?FDA label uses
- Is Latuda a controlled substance?Federal schedule
- Atypical Antipsychotics listFDA drug class
- NDC 63402-302Lurasidone NDC record
- NDC 63402-304Lurasidone NDC record
- NDC 63402-306Lurasidone NDC record