Active Ingredient(s): Flurbiprofen
FDA Approved: * December 31, 1986
Pharm Company: * ALLERGAN
Category: Arthritis

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Ocufen Overview

Flurbiprofen is a member of the phenylalkanoic acid derivative family of nonsteroidal anti-inflammatory drugs (NSAIDs). It is primarily indicated as a pre-operative anti-miotic (in an ophthalmic solution) as well as orally for arthritis or dental pain. Side effects are analogous to those of ibuprofen.[1] It was derived from propionic acid by the research arm of Boots UK during the 1960s, a period which also included the discovery of ibuprofen, indometacin, diclofenac, naproxen...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Flurbiprofen

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Possible Dosages for this and Related Drugs:

  • Solution: 0.03%
  • Solution/drops: 0.03%
  • Tablet: 100mg, 50mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Ocufen: (2 results)

Sorted by National Drug Code
  • 11980-801 Ocufen .3 mg/ml Ophthalmic Solution/ Drops by Allergan, Inc.
  • 54868-1158 Ocufen .3 mg/ml Ophthalmic Solution/ Drops by Physicians Total Care, Inc.

Other drugs which contain Flurbiprofen or a similar ingredient: (2 results)