0025-1381 : Daypro 600 mg Oral Tablet


NDC: 0025-1381
Labeler: G.d. Searle LLC Division of Pfizer Inc
Product Type: Human Prescription Drug
Drug Name:  Daypro
Dosage Form: Oral Tablet, Film Coated
Application #: NDA018841
Rev. Date: 


Appearance:


Markings: DAYPRO;1381
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.

DAYPRO 1381: (0025-1381) Daypro 600 mg Oral Tablet by G.d. Searle LLC Division of Pfizer 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:

  • 0025-1381-31: 100 TABLET, FILM COATED IN 1 BOTTLE (0025‑1381‑31)
  • 0025-1381-34: 100 TABLET, FILM COATED IN 1 BOX, UNIT‑DOSE (0025‑1381‑34)
  • 0025-1381-51: 500 TABLET, FILM COATED IN 1 BOTTLE (0025‑1381‑51)

Active Ingredients:

  • Oxaprozin

Dosage Strength:

  • 600 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Hypromelloses
  • Methylcellulose (100 Mpa.s)
  • Magnesium Stearate
  • Polacrilin Potassium
  • Polyethylene Glycols
  • Titanium Dioxide

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 55289-453 Daypro 600 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 0025-1381 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.