Nabumetone
- Product NDC
- 33261-078
- 11-digit product format
- 332610078
- Labeler code
- 33261
- Product ID
- 33261-078_b3102c1a-a63f-480c-9391-99669c295f7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2008-03-01
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 33261-078-30 | Nabumetone | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 1 |
| 33261-078-60 | Nabumetone | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | | 1 |
| 33261-078-97 | Nabumetone | 126 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 126 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33261-078 | NABUMETONE TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20140128_fcf0a35b-1679-4c13-abde-7afc7d560484.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33261-078-30 | 33261007830 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 33261-078-60 | 33261007860 | 60 in 1 BOTTLE, PLASTIC | Historical |
| 33261-078-97 | 33261007897 | 126 in 1 BOTTLE, PLASTIC | Historical |