Quick answers
- What is Neoprofen?
- Neoprofen is a brand name of Ibuprofen lysine, a prescription medicine. The FDA NDC Directory lists 1 Neoprofen product in 1 strength and form.
- Who makes Neoprofen?
- Recordati Rare holds the FDA application for Neoprofen (NDA021903, approved April 13, 2006).
- Is there a generic or store brand of Neoprofen?
- Yes. The FDA NDC Directory lists 2 other products with the same active ingredients, strength and form as a Neoprofen product, 2 of them generic. Ask your pharmacist whether one is right for you.
- Has Neoprofen been recalled?
- No recall linked to Neoprofen products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Neoprofen is
Each Neoprofen 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.
Ibuprofen lysine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| ibuprofen lysine 10 mg/mL solution (intravenous) | Neoprofen | 2 products, 2 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Ibuprofen lysine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021903 | Recordati Rare | April 13, 2006 | 1 |
Companies that list Neoprofen
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Neoprofen products.
- Recordati Rare Diseases Inc.1 product
Recalls
No recall linked to Neoprofen 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.