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Loratadine by McKesson Contract Packaging

Medically reviewed on November 13, 2017

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: McKesson Contract Packaging
NDC Code: 76237-201

Drug Facts

Active Ingredient (in each tablet)

Loratadine, USP 10 mg

Purpose

Antihistamine

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 over1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other Information
  • Safety sealed: do not use if the imprinted bottle seal is open or torn.

  • Store at 20°-25°C (68°-77°F) (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

10 mg Label

NDC 76237-201-30

Loratadine Tablets, USP 10 mg Antihistamine

Drug Facts: Active ingredient (in each tablet)

Loratadine, USP 10 mg - Antihistamine

Non-Drowsy when taken as directed

WARNING: Keep out of reach of children

Store at 20° to 25°C (68° to 77°F)

[See USP for controlled room temperature]

LORATADINE 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76237-201(NDC:0781-5077)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
CELLULOSE, MICROCRYSTALLINE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
Product Characteristics
ColorWHITE (white to off white) Scoreno score
ShapeROUNDSize6mm
FlavorImprint CodeGG296
Contains    
Packaging
#Item CodePackage Description
1NDC:76237-201-306 BLISTER PACK in 1 BOX, UNIT-DOSE
15 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520909/26/2011
Labeler - McKesson Contract Packaging (968953377)
Registrant - McKesson Packaging Services a business unit of McKesson Corporation (140529962)
Establishment
NameAddressID/FEIOperations
McKesson Packaging Services a business unit of McKesson Corporation140529962REPACK(76237-201)

 
McKesson Contract Packaging

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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