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Nabumetone
Active ingredient 6 prescription 6 with labelling
Overview
Source: NDC DirectoryIngredient name
NABUMETONE
Base moiety
NABUMETONE
RxNorm CUI
UNII
LW0TIW155Z
Medication products
7
Brand names
5
Dosage forms
3
FAERS reports
6,395 · not a risk measure
- Nabumetone Powder
- Nabumetone 1000 mg Nabumetone · Tablet, Film Coated
- Nabumetone 500 mg Nabumetone · Tablet, Film Coated
- Nabumetone 750 mg Nabumetone · Tablet, Film Coated
- RELAFEN DS Nabumetone · Tablet
- Nabumetone Tablet
- Nabumetone Tablet, Film Coated
Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.
By dosage form
| Dosage form | Products | Examples |
|---|---|---|
| TABLET, Film Coated | 4 | Nabumetone 1000 mg, Nabumetone 500 mg, Nabumetone 750 mg, Nabumetone |
| Tablet | 2 | RELAFEN DS, Nabumetone |
| Powder | 1 | Nabumetone |
Sources for this page
| Dataset | Agency | Used for |
|---|---|---|
| NDC Directory | FDA | Ingredient name, strengths, products, labelers, packages |
| DailyMed RxNorm mappings | NLM | RxNorm concept identifier (RxCUI) |
| FAERS | FDA | Adverse event report totals |