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Brand-name prescription medicine

Tigan

Generic name: Trimethobenzamide hydrochloride

FDA application holder: PH Health

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Tigan?
Tigan is a brand name of Trimethobenzamide hydrochloride, a prescription medicine. The FDA NDC Directory lists 2 Tigan products in 1 strength and form.
Who makes Tigan?
PH Health holds the FDA application for Tigan (NDA017530, approved July 12, 1974). 1 other company (repackagers or distributors) also list Tigan products.
Is there a generic or store brand of Tigan?
Yes. The FDA NDC Directory lists 2 other products with the same active ingredients, strength and form as a Tigan product, 1 of them generic. Ask your pharmacist whether one is right for you.
Has Tigan been recalled?
No recall linked to Tigan products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Tigan is

Each Tigan product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Trimethobenzamide hydrochloride · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
trimethobenzamide hydrochloride 100 mg/mL
injection (intramuscular)
Tigan 2 products, 2 companies DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Trimethobenzamide hydrochloride →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Tigan products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA017530PH HealthJuly 12, 19742

Companies that list Tigan

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Tigan products.

Recalls

No recall linked to Tigan products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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