71335-0393 : Oxaprozin 600 mg Oral Tablet, Film Coated


NDC: 71335-0393
Labeler: Bryant Ranch Prepack
Product Type: Human Prescription Drug
Drug Name:  Oxaprozin
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA075855
Rev. Date: 


Appearance:


Markings: C;01;70
Shapes:  Oval
Colors:  Yellow
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.

C 01 70: (55111-170) Oxaprozin 600 mg Oral Tablet, Film Coated by Bryant Ranch Prepack
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:

  • 71335-0393-1: 30 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑1)
  • 71335-0393-2: 20 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑2)
  • 71335-0393-3: 14 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑3)
  • 71335-0393-4: 60 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑4)
  • 71335-0393-5: 90 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑5)
  • 71335-0393-6: 6 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑6)
  • 71335-0393-7: 120 TABLET, FILM COATED IN 1 BOTTLE (71335‑0393‑7)

Active Ingredients:

  • Oxaprozin

Dosage Strength:

  • 600 mg

Inactive Ingredients:

  • Starch, Corn
  • D&c Yellow No. 10
  • Fd&c Yellow No. 6
  • Hypromellose, Unspecified
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Polydextrose
  • Polyethylene Glycol, Unspecified
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide
  • Triacetin

Pharmaceutical Classes:

  • Cyclooxygenase Inhibitors [MoA]
  • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Related Products:

Based on records with the same trade name.
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  • 63629-8724 Oxaprozin 600 mg Oral Tablet by Bryant Ranch Prepack
  • 72162-1051 Oxaprozin 600 mg Oral Tablet by Bryant Ranch Prepack
  • 0093-0924 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0185-0141 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Eon Labs, Inc.
  • 16590-178 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Stat Rx USA LLC
  • 21695-100 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Rebel Distributors Corp
  • 42291-662 Oxaprozin 600 mg/1 Oral Tablet by Avkare, Inc.
  • 49999-376 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 50090-2012 Oxaprozin 600 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 50436-2899 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Unit Dose Services
  • 52959-800 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by H.j. Harkins Company, Inc.
  • 54569-5212 Oxaprozin 600 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 54868-4548 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Physicians Total Care, Inc.
  • 55111-170 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Dr. Reddy's Laboratories Limited
  • 55289-601 Oxaprozin 600 mg (As Oxaprozin Potassium 678 mg) Oral Tablet by Pd-rx Pharmaceuticals, Inc.
  • 55466-140 Oxaprozin 600 mg Oral Tablet, Film Coated by Neolpharma, Inc.
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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.