Nabumetone
- Product NDC
- 76282-257
- 11-digit product format
- 762820257
- Labeler code
- 76282
- Product ID
- 76282-257_11f0008a-dff5-4fd3-8f48-76d033ea87f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Exelan Pharmaceuticals Inc.
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2015-04-14
- Substance
- NABUMETONE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nabumetone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NABUMETONE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LW0TIW155Z |
| Rxcui | 311892, 311893 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76282-257-01 | Nabumetone | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 11 |
| 76282-257-05 | Nabumetone | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 11 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NABUMETONE | ACTIVE INGREDIENT | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| NABUMETONE | ACTIVE MOIETY | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76282-257 | NABUMETONE TABLET, FILM COATED [EXELAN PHARMACEUTICALS INC.] | 11 | Current NDC, Legacy NDC, 2 package rows | 20250410_16e76e29-9315-40c0-b1d6-8d91961063cf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76282-257-01 | 76282025701 | 100 TABLET, FILM COATED in 1 BOTTLE (76282-257-01) | 2015-04-14 | 0000-00-00 | No | No | Current |
| 76282-257-05 | 76282025705 | 500 TABLET, FILM COATED in 1 BOTTLE (76282-257-05) | 2015-04-14 | 0000-00-00 | No | No | Current |