LORATADINE tablet

Երկիր: Ամերիկայի Միացյալ Նահանգներ

Լեզու: անգլերեն

Աղբյուրը: NLM (National Library of Medicine)

Ակտիվ բաղադրիչ:

LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)

Հասանելի է:

NCS HealthCare of KY, Inc dba Vangard Labs

INN (Միջազգային անվանումը):

LORATADINE

Կազմը:

LORATADINE 10 mg

Կառավարման երթուղին:

ORAL

Ռեկվիզորի տեսակը:

OTC DRUG

Թերապեւտիկ ցուցումներ:

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

Լիազորման կարգավիճակը:

Abbreviated New Drug Application

Ապրանքի հատկությունները

LORATADINE- LORATADINE TABLET
NCS HEALTHCARE OF KY, INC DBA VANGARD LABS
----------
DRUG FACTS
ACTIVE INGREDIENT (IN EACH TABLET)
Loratadine, USP 10 mg
PURPOS E
Antihistamine
US ES
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
liver or kidney disease.Your doctor should determine if you need a
different dose.
WHEN USING THIS PRODUCT
do not take more than directed. Taking more than directed may cause
drowsiness.
STOP USE AND ASK A 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 6 years and over
1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of age
ask a doctor
consumers with liver or kidney disease ask a doctor
OTHER INFORMATION
Safety sealed: do not use if the imprinted bottle seal is open or
torn.
Store at 20º - 25ºC (68º - 77ºF) (see USP Controlled Room
Temperature)..
INACTIVE INGREDIENTS
Lactose monohydrate, magnesium stearate, microcrystalline cellulose
and sodium starch glycolate.
QUESTIONS OR COMMENTS?
1-800-525-8747
03-2008M
Sandoz Inc.
Princeton, NJ 08540
PRINCIPAL DISPLAY PANEL
Loratadine Tablets, USP 10mg
LORATADINE
loratadine tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:0 6 15-558 6 (NDC:0 78 1-50 77)
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
LO RATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)
LORATADINE
10 mg
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
LACTO SE MO NO HYDRATE (UNII: EWQ57Q8 I5X)
NCS HealthCare of KY, Inc dba Vangard Labs
MAGNESIUM STEARATE (UNII: