lurasidone hydrochloride
- Product NDC
- 0904-7357
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lurasidone hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA212244
- Marketing category
- ANDA
- Substance
- LURASIDONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0904-7357-61 | 100 BLISTER PACK in 1 CARTON (0904-7357-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 2023-02-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| lurasidone hydrochloride | Major Pharmaceuticals | 2025-09-11 | HUMAN PRESCRIPTION DRUG LABEL | 5 |