0093-0924 : Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet


NDC: 0093-0924
Labeler: Teva Pharmaceuticals USA Inc
Product Type: Human Prescription Drug
Drug Name:  Oxaprozin
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA075849
Rev. Date: 


Appearance:


Markings: 9;3;0924
Shapes:  Oval
Colors:  White
Size (mm): 19
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

9 3 0924: (0093-0924) Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
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:

  • 0093-0924-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0093‑0924‑01)
  • 0093-0924-05: 500 TABLET, FILM COATED IN 1 BOTTLE (0093‑0924‑05)

Active Ingredients:

  • Oxaprozin

Dosage Strength:

  • 600 mg

Inactive Ingredients:

  • Carnauba Wax
  • Hypromelloses
  • Magnesium Stearate
  • Methylcellulose (15 Cps)
  • Cellulose, Microcrystalline
  • Polacrilin Potassium
  • Polyethylene Glycols
  • Polysorbate 80
  • Starch, Corn
  • Titanium Dioxide

Pharmaceutical Classes:

  • Cyclooxygenase Inhibitors [MoA]
  • Anti-Inflammatory Agents
  • Non-Steroidal [CS]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Related Products:

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NDC QR Code

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NDC 0093-0924 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.