Quick answers
- What is Trifluoperazine hydrochloride used for?
- The FDA-approved label (Trifluoperazine Hydrochloride, Remedyrepack Inc., June 30, 2026) says: “For the management of schizophrenia. Trifluoperazine HCl is effective for the short-term treatment of generalized non-psychotic anxiety. However, trifluoperazine HCl is not the first drug to be used in therapy for most patients with non-psychotic anxiety because certain risks associated with its use are not shared by common alternative treatments (i.e., benzodiazepines). …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Trifluoperazine hydrochloride have a boxed warning?
- Yes. The FDA label for Trifluoperazine Hydrochloride has a boxed warning, the FDA’s strongest warning. Read it on the full label and ask your pharmacist.
- Is there a shortage of Trifluoperazine hydrochloride?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Trifluoperazine hydrochloride been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Trifluoperazine hydrochloride?
- 6 companies list prescription products of Trifluoperazine hydrochloride in the FDA NDC Directory, including Mylan Institutional Inc., Sandoz Inc and Safecor Health LLC.
What Trifluoperazine hydrochloride is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
For the management of schizophrenia. Trifluoperazine HCl is effective for the short-term treatment of generalized non-psychotic anxiety. However, trifluoperazine HCl is not the first drug to be used in therapy for most patients with non-psychotic anxiety because certain risks associated with its use are not shared by common alternative treatments (i.e., benzodiazepines). …
— FDA label: Trifluoperazine Hydrochloride, Remedyrepack Inc., effective June 30, 2026. Read the full label on DailyMed →
The FDA has 11 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Conditions named on the label
These condition names appear word for word in the label’s “Indications and Usage” text (matched with a reviewed table). Each page lists hospitals whose own websites name the condition.
Related medical specialties
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
This label has a boxed warning. Read it on the full label →
11 of 11 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Tablet, film coated |
|---|---|
| Route | Oral |
| Prescription products | 24 in the FDA NDC Directory |
What pharmacies pay (NADAC)
The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.
This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.
| Strength and form | Generic or brand | Pharmacies pay |
|---|---|---|
| trifluoperazine hydrochloride 1 mg tablet, film coated | Generic | $0.4047 per tablet |
| trifluoperazine hydrochloride 10 mg tablet, film coated | Generic | $1.24 per tablet |
| trifluoperazine hydrochloride 2 mg tablet, film coated | Generic | $0.5353 per tablet |
| trifluoperazine hydrochloride 5 mg tablet, film coated | Generic | $0.7562 per tablet |
NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.
Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Mylan Institutional Inc.4 products
- Sandoz Inc4 products
- Safecor Health LLC4 products
- Bryant Ranch Prepack4 products
- Remedyrepack Inc.4 products
- Mylan Pharmaceuticals Inc.4 products
FDA approval history
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
Generic approvals (5)
- ANDA085785Sandoz · November 20, 1981
- ANDA085786Sandoz · November 20, 1981
- ANDA085788Sandoz · November 20, 1981
- ANDA085789Sandoz · November 20, 1981
- ANDA040209Mylan · July 7, 1997
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 198322, 198323, 198324, 198325 |
|---|---|
| SPL set ID of the quoted label | f789e8f4-7ed2-4cac-b1b1-5068690cd0ed |
| FDA labels (SPL) | 11 |
| FDA applications | 5 ANDA |
| Active ingredients (FDA) | TRIFLUOPERAZINE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Trifluoperazine Hydrochloride, Remedyrepack Inc., effective June 30, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →