NDC 31722-083 – Lurasidone Hydrochloride
Lurasidone Hydrochloride 80 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-083
Product details
- Brand name
- Lurasidone Hydrochloride
- Generic name
- Lurasidone Hydrochloride
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA218174
- Marketed since
- August 21, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 80 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-083-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-083-05) | Aug 21, 2024 |
| 31722-083-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-083-30) | Aug 21, 2024 |
| 31722-083-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-083-90) | Aug 21, 2024 |
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