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Brand-name prescription medicine

Vybrique

Generic name: Sildenafil

FDA application holder: Ibsa

Strengths and generic versions Official label

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.

At a glance

4Strengths and forms
4Same medicine, other names
2025FDA approval
0Recalls (FDA reports)

Quick answers

What is Vybrique?
Vybrique is a brand name of Sildenafil, a prescription medicine. The FDA NDC Directory lists 4 Vybrique products in 4 strengths and forms.
Who makes Vybrique?
Ibsa holds the FDA application for Vybrique (NDA210858, approved December 16, 2025).
Is there a generic or store brand of Vybrique?
Yes. The FDA NDC Directory lists 4 other products with the same active ingredients, strength and form as a Vybrique product. Ask your pharmacist whether one is right for you.
Has Vybrique been recalled?
No recall linked to Vybrique products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Vybrique is

Each Vybrique 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.

Sildenafil · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
sildenafil citrate 100 mg
film (oral)		 Vybrique 1 product, 1 company DailyMed
sildenafil citrate 25 mg
film (oral)		 Vybrique 1 product, 1 company DailyMed
sildenafil citrate 50 mg
film (oral)		 Vybrique 1 product, 1 company DailyMed
sildenafil citrate 75 mg
film (oral)		 Vybrique 1 product, 1 company DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Vybrique products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA210858IbsaDecember 16, 20254

Companies that list Vybrique

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

Recalls

No recall linked to Vybrique 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.

Report an error → · Information for medicine makers