Nabumetone
- Product NDC
- 60760-386
- 11-digit product format
- 607600386
- Labeler code
- 60760
- Product ID
- 60760-386_f04754bc-d97e-2ee5-e053-2a95a90a397a
- 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
- 2018-07-19
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 500 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 |
|---|
| 60760-386-15 | 60760038615 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-386-15) | 2018-07-19 | 0000-00-00 | No | No | Current |
| 60760-386-60 | 60760038660 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-386-60) | 2019-08-21 | 0000-00-00 | No | No | Current |