NDC 70771-1735 – Lurasidone hydrochloride
Lurasidone Hydrochloride 40 mg/1 · Tablet, Coated · Oral
Product NDC70771-1735
Product details
- Brand name
- Lurasidone hydrochloride
- Generic name
- Lurasidone hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208052
- Marketed since
- February 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1735-1 | 100 TABLET, COATED in 1 BOTTLE (70771-1735-1) | Feb 1, 2023 |
| 70771-1735-3 | 30 TABLET, COATED in 1 BOTTLE (70771-1735-3) | Mar 23, 2023 |
| 70771-1735-4 | 10 BLISTER PACK in 1 CARTON (70771-1735-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1735-2) | Feb 1, 2023 |
| 70771-1735-5 | 500 TABLET, COATED in 1 BOTTLE (70771-1735-5) | Feb 1, 2023 |
| 70771-1735-9 | 90 TABLET, COATED in 1 BOTTLE (70771-1735-9) | Feb 1, 2023 |
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