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

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Fexofenadine Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

FEXOFENADINE HYDROCHLORIDE DESCRIPTION


Fexofenadine Hydrochloride





CLINICAL PHARMACOLOGY

Mechanism of Action:


PHARMACOKINETICS

Absorption:


Distribution:


Elimination:



Metabolism:


Special Populations:


Seasonal allergic rhinitis (SAR) and chronic idiopathic urticaria (CIU) patients:


Geriatric Subjects:


Pediatric Patients:


Renal Impairment:


Hepatic Impairment:


Effect of Gender:


PHARMACODYNAMICS

Wheal and Flare:



Effects on QTC:



CLINICAL STUDIES

Seasonal Allergic Rhinitis:

Adults:



Pediatrics:



Chronic Idiopathic Urticaria:


INDICATIONS & USAGE

Seasonal Allergic Rhinitis:


Chronic Idiopathic Urticaria:


FEXOFENADINE HYDROCHLORIDE CONTRAINDICATIONS



PRECAUTIONS

Drug Interaction with Erythromycin and Ketoconazole:






Drug Interactions with Antacids:


CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY





PREGNANCY

Teratogenic Effects:

Category C:



Nonteratogenic Effects:


NURSING MOTHERS



PEDIATRIC USE






GERIATRIC USE



FEXOFENADINE HYDROCHLORIDE ADVERSE REACTIONS


Seasonal Allergic Rhinitis:

Adults:







Pediatric:





Chronic Idiopathic Urticaria:





OVERDOSAGE






DOSAGE & ADMINISTRATION

Seasonal Allergic Rhinitis:

Adults and Children 12 Years and Older:


Children 6 to 11 Years:


Chronic Idiopathic Urticaria:

Adults and Children 12 Years and Older:


Children 6 to 11 Years:


HOW SUPPLIED






STORAGE AND HANDLING




INFORMATION FOR PATIENTS


  • ●     Fexofenadine hydrochloride tablets are prescribed for the relief of symptoms of seasonal allergic rhinitis or for the relief of symptoms of chronic idiopathic urticaria (hives). Instruct patients to take fexofenadine hydrochloride tablets only as prescribed. Do not exceed the recommended dose. If any untoward effects occur while taking fexofenadine hydrochloride tablets, discontinue use and consult a doctor.
  • ●     Patients who are hypersensitive to any of the ingredients should not use these products.
  • ●     Patients who are pregnant or nursing should use these products only if the potential benefit justifies the potential risk to the fetus or nursing infant.
  • ●     Advise patients and parents/caregivers of pediatric patients to store the medication in a tightly closed container in a cool, dry place, away from small children.
  • ●     Advise patients and parents/caregivers not to take fexofenadine hydrochloride tablets with fruit juices.
  • ●     Advise patients to take the fexofenadine hydrochloride tablets with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Fexofenadine Hydrochloride

Fexofenadine Hydrochloride

Fexofenadine Hydrochloride

Fexofenadine Hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-286(NDC:0093-7252)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FEXOFENADINE HYDROCHLORIDE FEXOFENADINE 60 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
FERROSOFERRIC OXIDE
ferric oxide red
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol
povidone
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
orange 9 mm 93;7252 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-286-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076447 2011-08-22


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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