NDC 46708-498 – Lurasidone Hydrochloride
Lurasidone Hydrochloride 120 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-498
Product details
- Brand name
- Lurasidone Hydrochloride
- Generic name
- Lurasidone Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213248
- Marketed since
- January 24, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 120 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 46708-498-10 | 100 BLISTER PACK in 1 CARTON (46708-498-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jan 24, 2023 |
| 46708-498-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-498-30) | Jan 24, 2023 |
| 46708-498-71 | 500 TABLET, FILM COATED in 1 BOTTLE (46708-498-71) | Jan 24, 2023 |
| 46708-498-90 | 90 TABLET, FILM COATED in 1 BOTTLE (46708-498-90) | Jan 24, 2023 |
| 46708-498-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-498-91) | Jan 24, 2023 |
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- 62332-496 Lurasidone Hydrochloride 60 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.
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