Lurasidone hydrochloride
- Product NDC
- 70518-4117
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lurasidone hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208047
- Marketing category
- ANDA
- Substance
- LURASIDONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70518-4117-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0) | 2024-06-27 | | No | Historical |
| 70518-4117-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4117-1) | 2025-08-23 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lurasidone hydrochloride | REMEDYREPACK INC. | 2025-08-25 | HUMAN PRESCRIPTION DRUG LABEL | 3 |