Nabumetone
- Product NDC
- 0185-0146
- 11-digit product format
- 001850146
- Labeler code
- 0185
- Product ID
- 0185-0146_ea45619f-82b6-46d6-bcea-ac43bbe44613
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumentone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA075280
- Marketing category
- ANDA
- Marketing start
- 2002-02-25
- Marketing end
- 2022-07-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0185-0146-01 | 00185014601 | 100 TABLET in 1 BOTTLE (0185-0146-01) | 100 tablet | 2002-02-25 | 2022-07-31 | No | No | Current |
| 0185-0146-05 | 00185014605 | 500 TABLET in 1 BOTTLE (0185-0146-05) | 500 tablet | 2002-02-25 | 2022-06-30 | No | No | Current |