Hydroxyzine Hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Hydroxyzine Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

HYDROXYZINE HYDROCHLORIDE DESCRIPTION


Hydroxyzine Hydrochloride





CLINICAL PHARMACOLOGY






INDICATIONS & USAGE






HYDROXYZINE HYDROCHLORIDE CONTRAINDICATIONS




WARNINGS

WARNINGS

Nursing Mothers


PRECAUTIONS




GERIATRIC USE

Geriatric Use




HYDROXYZINE HYDROCHLORIDE ADVERSE REACTIONS









OVERDOSAGE

OVERDOSAGE




DOSAGE & ADMINISTRATION







HOW SUPPLIED

















INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
ANHYDROUS LACTOSE

CARNAUBA WAX
SILICON DIOXIDE
CROSPOVIDONE
HYPROMELLOSES
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE

POLYDEXTROSE
POLYETHYLENE GLYCOL
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
TRIACETIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Hydroxyzine Hydrochloride

Hydroxyzine Hydrochloride

Hydroxyzine Hydrochloride

Hydroxyzine Hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-696(NDC:50111-308)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYDROXYZINE HYDROCHLORIDE HYDROXYZINE 25 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS LACTOSE
carnauba wax
SILICON DIOXIDE
CROSPOVIDONE
HYPROMELLOSES
MAGNESIUM STEARATE
cellulose, microcrystalline
POLYDEXTROSE
polyethylene glycol
SODIUM STARCH GLYCOLATE TYPE A POTATO
titanium dioxide
triacetin

Product Characteristics

Color Size Imprint Code Shape
white 6 mm PA;308 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-696-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088618 2011-03-30


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