FEXOFENADINE HYDROCHLORIDE tablet

Quốc gia: Hoa Kỳ

Ngôn ngữ: Tiếng Anh

Nguồn: NLM (National Library of Medicine)

Thành phần hoạt chất:

Fexofenadine Hydrochloride (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)

Sẵn có từ:

Dr. Reddy's Laboratories Inc.

Tuyến hành chính:

ORAL

Loại thuốc theo toa:

OTC DRUG

Chỉ dẫn điều trị:

Antihistamine 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

Tình trạng ủy quyền:

Abbreviated New Drug Application

Đặc tính sản phẩm

FEXOFENADINE HYDROCHLORIDE- FEXOFENADINE HYDROCHLORIDE TABLET
DR. REDDY'S LABORATORIES INC.
----------
FEXOFENADINE HCL TABLETS USP
ACTIVE INGREDIENT(S)
Fexofenadine HCl USP, 60 mg
PURPOSE
Antihistamine
USE(S)
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
if you have ever had an allergic reaction to this product or any of
its ingredients.
ASK A DOCTOR BEFORE USE IF YOU HAVE
kidney disease. Your doctor should determine if you need a different
dose.
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 DOCTOR IF
an allergic reaction to this product occurs. Seek medical help right
away.
IF PREGNANT OR BREAST-FEEDING,
ask a health professional before use.
KEEP OUT OF REACH OF CHILDREN.
In case of overdose, get medical help or contact a Poison Control
Center right away.
DIRECTIONS
adults and children 12 years
of age and over
take one 60 mg tablet with water every 12 hours; do not
take more than2 tablets 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
OTHER INFORMATION
safety sealed: do not use if carton is opened or if printed foil inner
seal on bottle is
torn or missing
store between 20° and 25°C (68° and 77°F)
protect from excessive moisture
this product meets the requirements of USP Dissolution Test 4
INACTIVE INGREDIENTS
colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C
Red no. 40,
hypromellose, iron oxide black, magnesium stearate, mannitol,
polyethylene glycol,
powder cellulose and titanium dioxide
QUESTIONS?
Call 1-888-375-3784
PACKAGE LABEL PRINCIPAL DISPLAY PANEL SECTION
Container:
Carton:
FEXOFENADINE HYDROCHLORIDE
fexofenadine hydrochloride tablet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:43598-936(NDC:5511