NDC 33342-422 – Lurasidone hydrochloride
Lurasidone Hydrochloride 80 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-422
Product details
- Brand name
- Lurasidone hydrochloride
- Generic name
- Lurasidone hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212124
- Marketed since
- June 9, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 80 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 33342-422-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-422-07) | Jun 9, 2023 |
| 33342-422-10 | 90 TABLET, FILM COATED in 1 BOTTLE (33342-422-10) | Jun 9, 2023 |
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