Quick answers
- What is Rugby All Day Relief?
- Rugby All Day Relief is a brand name of Naproxen, a prescription medicine. The FDA NDC Directory lists 1 Rugby All Day Relief product in 1 strength and form.
- Who makes Rugby All Day Relief?
- Perrigo holds the FDA application for Rugby All Day Relief (ANDA074661, approved January 13, 1997).
- Is there a generic or store brand of Rugby All Day Relief?
- Other products of Naproxen are listed with the FDA, but none in exactly the same strength and form as a Rugby All Day Relief product.
- Has Rugby All Day Relief been recalled?
- No recall linked to Rugby All Day Relief products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Rugby All Day Relief is
Each Rugby All Day Relief 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.
Naproxen · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| naproxen sodium 220 mg tablet, film coated (oral) | Rugby All Day Relief | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Naproxen →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA074661 | Perrigo | January 13, 1997 | 1 |
Companies that list Rugby All Day Relief
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Rugby All Day Relief products.
- Bryant Ranch Prepack1 product
Recalls
No recall linked to Rugby All Day Relief 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.