60687-374 : Nabumetone 500 mg Oral Tablet, Film Coated


NDC: 60687-374
Labeler: American Health Packaging
Product Type: Human Prescription Drug
Drug Name:  Nabumetone
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA091083
Rev. Date: 


Appearance:


Markings: 3670
Shapes:  Oval
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.

3670: (60687-374) Nabumetone 500 mg Oral Tablet, Film Coated by American Health Packaging
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 60687-374-01: 100 BLISTER PACK IN 1 BOX, UNIT‑DOSE (60687‑374‑01) > 1 TABLET, FILM COATED IN 1 BLISTER PACK (60687‑374‑11)

Active Ingredients:

  • Nabumetone

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Starch, Corn
  • Hypromellose, Unspecified
  • Magnesium Stearate
  • Povidone, Unspecified
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide
  • Triacetin
  • Talc /

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.
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NDC QR Code

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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.