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Brand-name prescription medicine

Glatopa

Generic name: Glatiramer acetate

FDA application holder: Sandoz

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 Glatopa?
Glatopa is a brand name of Glatiramer acetate, a prescription medicine. The FDA NDC Directory lists 4 Glatopa products in 2 strengths and forms.
Who makes Glatopa?
Sandoz holds the FDA application for Glatopa (ANDA090218, approved April 16, 2015). 1 other company (repackagers or distributors) also list Glatopa products.
Is there a generic or store brand of Glatopa?
Yes. The FDA NDC Directory lists 14 other products with the same active ingredients, strength and form as a Glatopa product, 12 of them generic. Ask your pharmacist whether one is right for you.
What do pharmacies pay for Glatopa?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 2 Glatopa strengths and forms (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 Glatopa been recalled?
No recall linked to Glatopa products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Glatopa is

Each Glatopa 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.

Glatiramer acetate · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
glatiramer acetate 20 mg/mL
injection, solution (subcutaneous)
Glatopa 7 products, 7 companies DailyMed
glatiramer acetate 40 mg/mL
injection, solution (subcutaneous)
Glatopa 7 products, 7 companies DailyMed

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

FDA approval

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
FDA applications of Glatopa products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
ANDA090218SandozApril 16, 20152
ANDA206921SandozFebruary 12, 20182

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 Glatopa, by strength and form
Strength and formGeneric or brandPharmacies pay
glatiramer acetate 20 mg/mL
injection, solution
Generic: Glatopa $39.67 per mL
Generic of the same strength and form: $39.67 per mL
glatiramer acetate 40 mg/mL
injection, solution
Generic: Glatopa $82.23 per mL
Generic of the same strength and form: $82.23 per mL

NADAC list of November 4, 2026; these prices took effect on October 21, 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 Glatopa

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

Recalls

No recall linked to Glatopa 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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