Nabumetone
- Product NDC
- 68084-051
- 11-digit product format
- 680840051
- Labeler code
- 68084
- Product ID
- 68084-051_74305afa-21c8-188d-e053-2a91aa0a115a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumentone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075280
- Marketing category
- ANDA
- Marketing start
- 2013-10-21
- Marketing end
- 2020-02-29
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record