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

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Loratadine

Mylan Pharmaceuticals Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

(in each tablet)

Loratadine USP, 10 mg

Purpose

Antihistamine

Loratadine 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

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 of kidney disease

ask a doctor

Loratadine Other information

  • •Tamper Evident: do not use if foil seal under cap is missing, open or broken.
  • •store between 20° to 25°C (68° to 77°F)
  • •protect from excessive moisture

Inactive ingredients

Corn starch, lactose monohydrate and magnesium stearate.

Questions or comments?

call 1-877-446-3679 (1-877-4-INFO-RX)

Manufactured for:
Mylan Pharmaceuticals Inc.
Morgantown, WV 26505 U.S.A.

Made in India
Code No.: MH/DRUGS/25/NKD/89

PRODUCT PACKAGING

NDC 0378-8880-93

Original Prescription Strength

Non-Drowsy*

Loratadine
Tablets USP, 10 mg

Antihistamine

Indoor and Outdoor Allergies

24 Hour Relief of:

  • Sneezing
  • Runny Nose
  • Itchy, Watery Eyes
  • Itchy Throat or Nose

*When taken as directed. See Drug Facts Panel.

RMX8880H1

30 Tablets

Loratadine

loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0378-8880
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

Product Characteristics

Color Size Imprint Code Shape
WHITE (white to off-white) 6 mm G;L;10 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0378-8880-93 30 in 1 BOTTLE, PLASTIC
2 NDC:0378-8880-10 1000 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076154 2013-03-27


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