Upper Respiratory Allergies
ZUTRIPRO Oral Solution is indicated for relief of symptoms including nasal congestion associated with upper respiratory allergies in adults 18 years of age and older.
Important Limitations of Use
Not indicated for pediatric patients under 18 years of age [see Pediatric Use].
DOSAGE AND ADMINISTRATION
Administer ZUTRIPRO Oral Solution by the oral route only. Measure ZUTRIPRO Oral Solution with an accurate milliliter measuring device. Do not use a household teaspoon to measure the dose [see WARNINGS AND PRECAUTIONS].
Adults 18 Years of Age and Older
5 mL every 4 to 6 hours as needed, not to exceed 4 doses (20 mL) in 24 hours.
Dosage Forms and Strengths
ZUTRIPRO is a clear, colorless to light yellow, grape-flavored liquid.
5 mL of ZUTRIPRO Oral Solution contains: hydrocodone bitartrate, USP, 5 mg; chlorpheniramine maleate, USP, 4 mg; and pseudoephedrine hydrochloride, USP, 60 mg [see DESCRIPTION].
ZUTRIPRO Oral Solution is supplied as a clear, colorless to light yellow, grape-flavored solution containing 5 mg hydrocodone bitartrate, 4 mg chlorpheniramine maleate, and 60 mg pseudoephedrine hydrochloride in each 5 mL. It is available in:
White HOPE bottles of one pint (480 mL): NDC 63717-876-16
Store solution at 20° to 25°C (68° to 77°F). [USP Controlled Room Temperature.]
Dispense in a tight, light-resistant container, as defined in the USP, with a child-resistant closure.
Manufactured for: Hawthorn Pharmaceuticals, Inc., Madison, MS 39110. Revised 06/2011
Last reviewed on RxList: 6/30/2011
This monograph has been modified to include the generic and brand name in many instances.
Additional Zutripro Information
- Zutripro Drug Interactions Center: cpm-pseudoephed-hydrocodone oral
- Zutripro Side Effects Center
- Zutripro FDA Approved Prescribing Information including Dosage
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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