NDC 43598-353 – Lurasidone hydrochloride
Lurasidone Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC43598-353
Product details
- Brand name
- Lurasidone hydrochloride
- Generic name
- Lurasidone hydrochloride
- Labeler
- Dr. Reddys Laboratories Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208047
- Marketed since
- February 20, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 43598-353-05 | 500 TABLET, FILM COATED in 1 BOTTLE (43598-353-05) | Feb 20, 2023 |
| 43598-353-30 | 30 TABLET, FILM COATED in 1 BOTTLE (43598-353-30) | Feb 20, 2023 |
| 43598-353-78 | 10 BLISTER PACK in 1 CARTON (43598-353-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-353-79) | Feb 20, 2023 |
| 43598-353-90 | 90 TABLET, FILM COATED in 1 BOTTLE (43598-353-90) | Feb 20, 2023 |
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