fexofenadine hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

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fexofenadine hydrochloride

Dispensing Solutions, Inc.
PSS World Medical, Inc.

Major Pharmaceuticals Fexofenadine Hydrochloride Tablets, 180 mg Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Fexofenadine HCl 180 mg

Purpose

Antihistamine

fexofenadine hydrochloride Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • itchy, watery eyes
  • sneezing
  • itching of the nose or throat

Warnings

Do not use



Ask a doctor before use if you have



When using this product

  • do not take more than directed
  • do not take at the same time as aluminum or magnesium antacids
  • do not take with fruit juices (see Directions)
Stop use and ask a doctor if



If pregnant or breast-feeding,


Keep out of reach of children.


Directions

adults and children 12 years of age and over
take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
children under 12 years of age
do not use
adults 65 years of age and older
ask a doctor
consumers with kidney disease
ask a doctor


fexofenadine hydrochloride Other information

  • do not use if blister unit is broken or torn (Use for Blister Configurations Only)
  • do not use if printed foil under cap is broken or missing (Use for Bottle Configurations Only)
  • store at 20°-25°C (68°-77°F)
  • protect from excessive moisture
  • this product meets the requirements of USP Dissolution Test 3

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, titanium dioxide

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel


fexofenadine hydrochloride

NDC 66336-0561-XX
NDC 66336-0561-30






























fexofenadine hydrochloride

fexofenadine hydrochloride TABLET, FILM COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:66336-561(NDC:0904-6214)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FEXOFENADINE HYDROCHLORIDE FEXOFENADINE 180 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
FERROSOFERRIC OXIDE
ferric oxide red
FERRIC OXIDE YELLOW
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
POLYETHYLENE GLYCOLS
povidone
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
orange (peach) 12 mm 93;7253 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66336-561-30 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076447 2011-04-14


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Be sure to consult your doctor before taking any medication!
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