Hydroxyzine Hydrochloride (Page 2 of 2)
DOSAGE AND ADMINISTRATION
For symptomatic relief of anxiety and tension associated with psychoneurosis and as an adjunct in organic disease states in which anxiety is manifested: in adults, 50 to 100 mg four times daily.: children under 6 years, 50 mg daily in divided doses: children over 6 years: 50 to 100 mg daily in divided doses.
For use in the management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses, and in histamine-mediated pruritus: in adults, 25 mg three times to four times daily.; children under 6 years, 50 mg daily in divided doses and children over 6 years, 50 to 100 mg daily in divided doses.
As a sedative when used as a premedication and following general anesthesia: 50 to 100 mg in adults, and 0.6 mg/kg in children.
When treatment is initiated by the intramuscular route of administration, subsequent doses may be administered orally.
As with all medications, the dosage should be adjusted according to the patient’s response to therapy.
HOW SUPPLIED
Hydroxyzine Hydrochloride Syrup (Hydroxyzine Hydrochloride Oral Solution, USP) 10 mg per 5 mL (teaspoonful) is a slightly yellow peppermint flavored liquid, supplied in 473 mL (16 fl. oz.) plastic bottles.
NDC 54838-502-80
Store at controlled room temperature 15° to 30°C (59° to 86°F). [See USP controlled room temperature].
Dispense in a tight, light-resistant container with child-resistant closure as defined in the USP.
Distributed by:
Lannett Company, Inc.
Philadelphia, PA 19136
10-1114
Rev. 01/23
473 mL label
NDC 54838-502-80
HydrOXYzine
Hydrochloride
Syrup
(HydrOXYzine Hydrochloride Oral Solution, USP)
10 mg per 5 mL
HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride solution | ||||||||||||||||||
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Labeler — Lannett Company, Inc. (002277481) |
Revised: 01/2023 Lannett Company, Inc.
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