Quick answers
- What is Evekeo?
- Evekeo is a brand name of Amphetamine, a prescription medicine. The FDA NDC Directory lists 2 Evekeo products in 2 strengths and forms.
- Who makes Evekeo?
- Azurity holds the FDA application for Evekeo (ANDA200166, approved August 9, 2012).
- Is there a generic or store brand of Evekeo?
- Yes. The FDA NDC Directory lists 33 other products with the same active ingredients, strength and form as a Evekeo product, 33 of them generic. Ask your pharmacist whether one is right for you.
- Has Evekeo been recalled?
- No recall linked to Evekeo products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Evekeo is
Each Evekeo 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.
Amphetamine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| amphetamine sulfate 10 mg tablet (oral) | Evekeo | 17 products, 11 companies | DailyMed |
| amphetamine sulfate 5 mg tablet (oral) | Evekeo | 16 products, 11 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Amphetamine →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA200166 | Azurity | August 9, 2012 | 2 |
Companies that list Evekeo
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Evekeo products.
- Azurity Pharmaceuticals, Inc.2 products
Recalls
No recall linked to Evekeo products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.