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

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Loratadine

Major Pharmaceuticals

Loratadine tablets


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Loratidine USP 10 mg

Purpose

Antihistamine

Use

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies, runny nose, itchy, watery eyes, sneezing, itching of the nose and throat.

Warning

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. You doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

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.

Pregnancy/breast-feeding warning

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 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

Loratadine Other information

Store at 20º - 25ºC (68º -77ºF); excursions permitted to 15o - 30o C (59o - 86o F). [ See USP Controlled Room Temperature]

Protect from excessive moisture.

Inactive ingredients

Corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch.

Questions?

Questions or comments? (800) 616-2471

Distributed by:

MAJOR® PHARMACEUTICALS

31778 Enterprise Drive, Livonia, MI  48150 USA

Re-Order No. 301592

PRINCIPAL DISPLAY PANEL LORATADINE TABLETS, USP 10MG

 Loratadine

Loratadine

Loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0904-6074(NDC:51660-526)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LORATADINE loratadine 10 mg

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
lactose monohydrate
MAGNESIUM STEARATE
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
WHITE 7 mm rx526 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0904-6074-61 100 in 1 BOX, UNIT-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076134 2010-06-15


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