NDC 67877-641 – Lurasidone hydrochloride
Lurasidone Hydrochloride 80 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-641
Product details
- Brand name
- Lurasidone hydrochloride
- Generic name
- Lurasidone hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212244
- Marketed since
- January 4, 2023
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-641-05 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-641-05) | Jan 4, 2023 |
| 67877-641-30 | 30 TABLET, FILM COATED in 1 BOTTLE (67877-641-30) | Jan 4, 2023 |
| 67877-641-38 | 10 BLISTER PACK in 1 CARTON (67877-641-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-641-33) | Jan 4, 2023 |
| 67877-641-90 | 90 TABLET, FILM COATED in 1 BOTTLE (67877-641-90) | Jan 4, 2023 |
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