NDC 23155-888 – Lurasidone Hydrochloride
Lurasidone Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral
Product NDC23155-888
Product details
- Brand name
- Lurasidone Hydrochloride
- Generic name
- Lurasidone Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208058
- Marketed since
- October 19, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 23155-888-03 | 30 TABLET, FILM COATED in 1 BOTTLE (23155-888-03) | Oct 19, 2023 |
| 23155-888-05 | 500 TABLET, FILM COATED in 1 BOTTLE (23155-888-05) | Aug 20, 2025 |
| 23155-888-09 | 90 TABLET, FILM COATED in 1 BOTTLE (23155-888-09) | Aug 20, 2025 |
| 23155-888-18 | 60500 TABLET, FILM COATED in 1 CONTAINER (23155-888-18) | Oct 19, 2023 |
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