NDC 47335-579 – Lurasidone Hydrochloride
Lurasidone Hydrochloride 120 mg/1 · Tablet · Oral
Product NDC47335-579
Product details
- Brand name
- Lurasidone Hydrochloride
- Generic name
- Lurasidone Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208066
- Marketed since
- February 20, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 120 mg/1
Uses, dosage, side effects and warnings for Lurasidone hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 47335-579-13 | 500 TABLET in 1 BOTTLE (47335-579-13) | Feb 20, 2023 |
| 47335-579-81 | 90 TABLET in 1 BOTTLE (47335-579-81) | Feb 20, 2023 |
Recalls mentioning this NDC
- D-0266-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment. - D-0267-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
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