NDC 0781-8032

Trifluoperazine Hydrochloride 2 mg tablet, film coated

On the label: Sandoz Inc..

Where it's 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
2 mg
Approval
ANDA ANDA085786
On the market since
Nov 20, 1981
Package NDCs
0781-8032-01
Official label
DailyMed (National Library of Medicine), updated Nov 30, 2024

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