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Brand-name prescription medicine

Pred Forte

Generic name: Prednisolone acetate

FDA application holder: Abbvie

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 Pred Forte?
Pred Forte is a brand name of Prednisolone acetate, a prescription medicine. The FDA NDC Directory lists 1 Pred Forte product in 1 strength and form.
Who makes Pred Forte?
Abbvie holds the FDA application for Pred Forte (NDA017011, approved May 30, 1973).
Is there a generic or store brand of Pred Forte?
Yes. The FDA NDC Directory lists 15 other products with the same active ingredients, strength and form as a Pred Forte product, 15 of them generic. Ask your pharmacist whether one is right for you.
What do pharmacies pay for Pred Forte?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 1 Pred 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 Pred Forte been recalled?
No recall linked to Pred Forte products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Pred Forte is

Each Pred 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.

Prednisolone acetate · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
prednisolone acetate 10 mg/mL
suspension/ drops (ophthalmic)
Pred Forte 15 products, 9 companies DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Pred Forte products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA017011AbbvieMay 30, 19731

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 Pred Forte, by strength and form
Strength and formGeneric or brandPharmacies pay
prednisolone acetate 10 mg/mL
suspension/ drops
Brand: Pred Forte $30.71 per mL
Generic of the same strength and form: $4.71–$5.06 per mL

NADAC list of November 4, 2026; these prices took effect on December 17, 2025. 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 Pred Forte

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

Recalls

No recall linked to Pred 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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