NDC 65162-879 – Lurasidone Hydrochloride
Lurasidone Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC65162-879
Product details
- Brand name
- Lurasidone Hydrochloride
- Generic name
- Lurasidone Hydrochloride
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208002
- Marketed since
- January 2, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65162-879-03 | 30 TABLET, COATED in 1 BOTTLE (65162-879-03) | Jan 2, 2023 |
| 65162-879-09 | 90 TABLET, COATED in 1 BOTTLE (65162-879-09) | Jan 2, 2023 |
| 65162-879-50 | 500 TABLET, COATED in 1 BOTTLE (65162-879-50) | Jan 2, 2023 |
Other Lurasidone hydrochloride products
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- 65162-881 Lurasidone Hydrochloride 80 mg/1 · Tablet, Coated · Amneal Pharmaceuticals LLC
- 65162-880 Lurasidone Hydrochloride 40 mg/1 · Tablet, Coated · Amneal Pharmaceuticals LLC
- 65162-882 Lurasidone Hydrochloride 120 mg/1 · Tablet, Coated · Amneal Pharmaceuticals LLC
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- 53746-881 Lurasidone Hydrochloride 80 mg/1 · Tablet, Coated · Amneal Pharmaceuticals of New York LLC
- 53746-082 Lurasidone Hydrochloride 60 mg/1 · Tablet, Coated · Amneal Pharmaceuticals of New York LLC
- 53746-880 Lurasidone Hydrochloride 40 mg/1 · Tablet, Coated · Amneal Pharmaceuticals of New York LLC
- 53746-879 Lurasidone Hydrochloride 20 mg/1 · Tablet, Coated · Amneal Pharmaceuticals of New York LLC
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- 70771-1736 Lurasidone Hydrochloride 60 mg/1 · Tablet, Coated · Zydus Lifesciences Limited
- 70771-1735 Lurasidone Hydrochloride 40 mg/1 · Tablet, Coated · Zydus Lifesciences Limited