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Brand-name prescription medicine

Epiduo Forte

Generic name: Adapalene and benzoyl peroxide

FDA application holder: Galderma Labs

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 Epiduo Forte?
Epiduo Forte is a brand name of Adapalene and benzoyl peroxide, a prescription medicine. The FDA NDC Directory lists 1 Epiduo Forte product in 1 strength and form.
Who makes Epiduo Forte?
Galderma Labs holds the FDA application for Epiduo Forte (NDA207917, approved July 15, 2015).
Is there a generic or store brand of Epiduo Forte?
Yes. The FDA NDC Directory lists 11 other products with the same active ingredients, strength and form as a Epiduo Forte product, 11 of them generic. Ask your pharmacist whether one is right for you.
What do pharmacies pay for Epiduo Forte?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 1 Epiduo Forte strength and form (see the table below). That is what pharmacies pay to buy it, not what you pay: your price depends on your insurance and your pharmacy.
Has Epiduo Forte been recalled?
No recall linked to Epiduo Forte products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Epiduo Forte is

Each Epiduo Forte 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.

Adapalene and benzoyl peroxide · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
adapalene 0.3% · benzoyl peroxide 2.5%
gel (topical)
Epiduo Forte 11 products, 10 companies DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Epiduo Forte products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA207917Galderma LabsJuly 15, 20151

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.

NADAC per unit for Epiduo Forte, by strength and form
Strength and formGeneric or brandPharmacies pay
adapalene 0.3% · benzoyl peroxide 2.5%
gel
Brand: Epiduo Forte $14.97 per gram
Generic of the same strength and form: $0.6474 per gram

NADAC list of November 4, 2026; these prices took effect on September 23, 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 Epiduo Forte

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

Recalls

No recall linked to Epiduo Forte 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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