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Brand-name prescription medicine

ChiRhoStim 40

Generic name: Human secretin

FDA application holder: Chirhoclin

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 ChiRhoStim 40?
ChiRhoStim 40 is a brand name of Human secretin, a prescription medicine. The FDA NDC Directory lists 1 ChiRhoStim 40 product in 1 strength and form.
Who makes ChiRhoStim 40?
Chirhoclin holds the FDA application for ChiRhoStim 40 (NDA021256, approved April 9, 2004).
Is there a generic or store brand of ChiRhoStim 40?
Other products of Human secretin are listed with the FDA, but none in exactly the same strength and form as a ChiRhoStim 40 product.
Has ChiRhoStim 40 been recalled?
No recall linked to ChiRhoStim 40 products (by their NDC code or label) appears in the FDA enforcement reports we use.

What ChiRhoStim 40 is

Each ChiRhoStim 40 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.

Human secretin · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
secretin human 40 ug/10 mL
injection, powder, lyophilized, for solution (intravenous)
ChiRhoStim 40 None listed DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of ChiRhoStim 40 products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA021256ChirhoclinApril 9, 20041

Companies that list ChiRhoStim 40

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of ChiRhoStim 40 products.

Recalls

No recall linked to ChiRhoStim 40 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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