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Daypro Alta

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Daypro Alta

Daypro Alta

INDICATIONS

Carefully consider the potential benefits and risks of DAYPRO ALTA (oxaprozin) and other treatment options before deciding to use DAYPRO ALTA (oxaprozin) . Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS).

DAYPRO ALTA (oxaprozin) is indicated:

DOSAGE AND ADMINISTRATION

Carefully consider the potential benefits and risks of DAYPRO ALTA (oxaprozin) and other treatment options before deciding to use DAYPRO ALTA (oxaprozin) . Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS).

After observing the response to initial therapy with DAYPRO ALTA (oxaprozin) , the dose and frequency should be adjusted to suit an individual patient's needs.

Osteoarthritis and Rheumatoid Arthritis: The recommended dose of DAYPRO ALTA for the relief of the signs and symptoms of osteoarthritis and rheumatoid arthritis is 1200 mg (two 600 mg tablets) once a day. Divided doses may be tried in patients unable to tolerate single doses. For osteoarthritis patients of low body weight of with milder disease, an initial dose of one 600 mg tablet once a day may be appropriate. The maximum total daily dose is 1200 mg.

HOW SUPPLIED

DAYPRO ALTA (oxaprozin) 600 mg tablets are blue, capsule-shaped, film-coated, with Searle 1391 printed on one side.

NDC Number Size
0025-5500-01 bottle of 100
0025-5500-03 bottle of 500
0025-5500-02 carton of 100 unit dose

Store at 25C (77F); excursions permitted to 15-30C (59-86F) (see USP Controlled Room Temperature) in tightly-closed container. Protect from moisture.

G.D. Searle LLC., Division of Pfizer Inc, NY, NY 10017. Revised January 2007. FDA Rev date: 7/5/2007

Last reviewed on RxList: 4/17/2008
This monograph has been modified to include the generic and brand name in many instances.

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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