NDC 50090-7078
lurasidone hydrochloride 20 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged from NDC 70436-093, made by Slate Run Pharmaceuticals, LLC (lurasidone hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants A-S Medication Solutions names for other drugs.
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA212091
- On the market since
- Feb 20, 2023
- Package NDCs
50090-7078-0- Official label
- DailyMed (National Library of Medicine), updated Feb 7, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?