NDC 23155-888-03
Lurasidone Hydrochloride 40 mg/1
Lurasidone Hydrochloride · TABLET, FILM COATED
Lurasidone Hydrochloride is a tablet, film coated containing lurasidone hydrochloride at a strength of 40 mg/1. Manufactured by Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc..
Key Facts
- Brand Name
- Lurasidone Hydrochloride
- Generic Name
- Lurasidone Hydrochloride
- NDC Code (Package)
23155-888-03- NDC Code (Product)
23155-888- Manufacturer
- Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.
- Strength
- 40 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA208058
- Marketing Start
- 10/19/2023
Recall History
No Recall HistoryView Full Drug Page
Lurasidone Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.