NDC 53746-879 – Lurasidone Hydrochloride
Lurasidone Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC53746-879
Product details
- Brand name
- Lurasidone Hydrochloride
- Generic name
- Lurasidone Hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208002
- Marketed since
- July 5, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 53746-879-30 | 30 TABLET, COATED in 1 BOTTLE (53746-879-30) | Jul 5, 2024 |
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