Nabumetone
- Product NDC
- 60760-387
- 11-digit product format
- 607600387
- Labeler code
- 60760
- Product ID
- 60760-387_f047ed59-6369-4cab-e053-2a95a90abffd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA091083
- Marketing category
- ANDA
- Marketing start
- 2019-04-12
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 60760-387-14 | 60760038714 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-387-14) | 2019-04-12 | 0000-00-00 | No | No | Current |
| 60760-387-60 | 60760038760 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-387-60) | 2019-04-12 | 0000-00-00 | No | No | Current |
| 60760-387-90 | 60760038790 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-387-90) | 2019-04-12 | 0000-00-00 | No | No | Current |