Nabumetone
- Product NDC
- 43063-859
- 11-digit product format
- 430630859
- Labeler code
- 43063
- Product ID
- 43063-859_e6d878d7-a0df-e4d5-e053-2995a90a04ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075189
- Marketing category
- ANDA
- Marketing start
- 2001-09-26
- 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 |
|---|
| 43063-859-40 | 43063085940 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-859-40) | 2018-06-08 | 0000-00-00 | No | No | Current |