August 27, 2016
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Daypro Alta

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Daypro Alta




Indications
Dosage
How Supplied

INDICATIONS

DAYPRO ALTA is indicated:

DOSAGE AND ADMINISTRATION

General Dosing Instructions

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

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

Divided doses may be tried in patients unable to tolerate single doses. For osteoarthritis patients of low body weight or 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.

Osteoarthritis

For OA, the dosage is 1200 mg (two 600 mg tablets) given orally once a day.

Rheumatoid Arthritis

For RA, the dosage is 1200 mg (two 600 mg tablets) given orally once a day.

HOW SUPPLIED

Dosage Forms And Strengths

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

Storage And Handling

DAYPRO ALTA 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 room temperature 20ºC to 25ºC (68ºF to 77ºF); excursions permitted between 15ºC to 30ºC (59ºF to 86ºF) (see USP Controlled Room Temperature). Dispense in a tightly-closed container. Protect from moisture.

Manufacture by: Pfizer Inc., 235 East 42nd Street, New York, NY, 10017. Revised May 2016

This monograph has been modified to include the generic and brand name in many instances.

Last reviewed on RxList: 6/21/2016

Indications
Dosage
How Supplied

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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