NDC 68382-966 – Lurasidone hydrochloride
Lurasidone Hydrochloride 40 mg/1 · Tablet, Coated · Oral
Product NDC68382-966
Product details
- Brand name
- Lurasidone hydrochloride
- Generic name
- Lurasidone hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208052
- Marketed since
- February 1, 2023
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 68382-966-01 | 100 TABLET, COATED in 1 BOTTLE (68382-966-01) | Feb 1, 2023 |
| 68382-966-05 | 500 TABLET, COATED in 1 BOTTLE (68382-966-05) | Feb 1, 2023 |
| 68382-966-06 | 30 TABLET, COATED in 1 BOTTLE (68382-966-06) | Mar 23, 2023 |
| 68382-966-16 | 90 TABLET, COATED in 1 BOTTLE (68382-966-16) | Feb 1, 2023 |
| 68382-966-77 | 100 BLISTER PACK in 1 CARTON (68382-966-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-966-30) | Feb 1, 2023 |
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