Nabumetone
- Product NDC
- 50090-1531
- 11-digit product format
- 500901531
- Labeler code
- 50090
- Product ID
- 50090-1531_e32895dd-bc6a-443b-8841-c530ee09f8a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2008-03-01
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 500 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1531-0 | 50090153100 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-1531-0) | 2014-12-15 | 0000-00-00 | No | No | Current |
| 50090-1531-4 | 50090153104 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-1531-4) | 2014-12-15 | 0000-00-00 | No | No | Current |
| 50090-1531-7 | 50090153107 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1531-7) | 2014-12-15 | 0000-00-00 | No | No | Current |