NDC 70518-4117 – Lurasidone hydrochloride
Lurasidone Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4117
Product details
- Brand name
- Lurasidone hydrochloride
- Generic name
- Lurasidone hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208047
- Marketed since
- June 27, 2024
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4117-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0) | Jun 27, 2024 |
| 70518-4117-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4117-1) | Aug 23, 2025 |
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