NDC 70518-4686
Trifluoperazine Hydrochloride 5 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Sandoz Inc.'s NDC 0781-8034.
Where the pills inside were made
This label doesn't name the factory that makes the drug. 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 Sandoz Inc. names for other drugs.
Product details
- Generic drug
- Trifluoperazine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA085789
- On the market since
- Jun 30, 2026
- Package NDCs
70518-4686-0- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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