0722-7077 : Nabumetone 750 mg 750 mg 750 mg Oral Tablet, Film Coated
| NDC: | 0722-7077 |
| Labeler: | Nexgen Pharma, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Nabumetone 750 mg |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA203166 |
| Rev. Date: |
Appearance:
| Markings: | HT;750 |
| Shapes: |
Capsule |
| Colors: |
 White |
| Size (mm): | 17 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 0722-7077-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0722‑7077‑01)
- 0722-7077-05: 500 TABLET, FILM COATED IN 1 BOTTLE (0722‑7077‑05)
Active Ingredients:
- Nabumetone
Dosage Strength:
- 750 mg
Pharmaceutical Classes:
- Cyclooxygenase Inhibitors [MoA]
- Anti-Inflammatory Agents
- Non-Steroidal [CS]
- Nonsteroidal Anti-inflammatory Drug [EPC]
Related Products:
Based on records with the same trade name.- 79739-7077 Nabumetone 750 mg Oral Tablet by Lgm Pharma Solutions, LLC
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.