Lurasidone Hydrochloride
- Product NDC
- 47335-579
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lurasidone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA208066
- Marketing category
- ANDA
- Substance
- LURASIDONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-579-13 | 500 TABLET in 1 BOTTLE (47335-579-13) | 2023-02-20 | | No | Historical |
| 47335-579-81 | 90 TABLET in 1 BOTTLE (47335-579-81) | 2023-02-20 | | No | Historical |
| 47335-579-83 | 30 TABLET in 1 BOTTLE (47335-579-83) | 2023-02-20 | | No | Historical |