NDC 23155-0501-05

Hydroxyzine hydrochloride 25 mg/1 TABLET

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NDC

23155-0501-05

Generic Name

Hydroxyzine hydrochloride

Brand Name

Hydroxyzine hydrochloride

Strength

25 mg/1

Dosage Form

TABLET

Route

ORAL

Package Size

—

Labeler

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE For symptomatic relief of anxiety and tension associated with psychoneurosis and as an adjunct in organic disease states in which anxiety is manifested. Useful in the management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses and in histamine-mediated pruritus. As a sedative when used as a premedication and following general anesthesia, hydroxyzine may potentiate meperidine and barbiturates, so their use in pre-anesthetic a…

Important Warnings

WARNINGS Nursing Mothers It is not known whether this drug is excreted in human milk. Since many drugs are so excreted, hydroxyzine should not be given to nursing mothers.

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other Hydroxyzine hydrochloride NDC Codes

23155-0501-0125 mg/1TABLET

2-Day

42806-0160-1025 mg/1TABLET, FILM COATED

2-Day

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