LURASIDONE HYDROCHLORIDE
- Product NDC
- 82804-215
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LURASIDONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208045
- Marketing category
- ANDA
- Substance
- LURASIDONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 82804-215-30 | 30 TABLET in 1 BOTTLE (82804-215-30) | 2025-03-31 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LURASIDONE HYDROCHLORIDE | Proficient Rx LP | 2025-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |