Nabumetone
- Product NDC
- 60760-015
- 11-digit product format
- 607600015
- Labeler code
- 60760
- Product ID
- 60760-015_7abcad3f-e3aa-18ff-e053-2a91aa0a7d74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St.Mary's Medical Park Pharmacy
- 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
- 2020-12-31
- 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 |
|---|
| 60760-015-15 | 60760001515 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-015-15) | 2018-02-02 | 0000-00-00 | No | No | Current |
| 60760-015-60 | 60760001560 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-015-60) | 2017-06-15 | 0000-00-00 | No | No | Current |