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Loratadine antihistamine by A-S Medication Solutions

Medically reviewed on October 26, 2017

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: A-S Medication Solutions
NDC Code: 50090-0836

Perrigo Loratadine Tablets, 10 mg Drug Facts

Active ingredient (in each tablet)

Loratadine 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. (1-800-222-1222)

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
do not use if printed foil under cap is broken or missing
store between 20° to 25°C (68° to 77°F)

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-800-719-9260

HOW SUPPLIED

Product: 50090-0836

NDC: 50090-0836-0 10 TABLET in a BOTTLE

NDC: 50090-0836-3 15 TABLET in a BOTTLE

NDC: 50090-0836-4 30 TABLET in a BOTTLE

NDC: 50090-0836-5 90 TABLET in a BOTTLE

NDC: 50090-0836-6 7 TABLET in a BOTTLE

NDC: 50090-0836-1 20 TABLET in a BOTTLE

Loratadine
LORATADINE  ANTIHISTAMINE
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50090-0836(NDC:45802-650)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
POVIDONE, UNSPECIFIED 
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize8mm
FlavorImprint CodeL612
Contains    
Packaging
#Item CodePackage Description
1NDC:50090-0836-0 10 TABLET in 1 BOTTLE
2NDC:50090-0836-3 15 TABLET in 1 BOTTLE
3NDC:50090-0836-4 30 TABLET in 1 BOTTLE
4NDC:50090-0836-5 90 TABLET in 1 BOTTLE
5NDC:50090-0836-6 7 TABLET in 1 BOTTLE
6NDC:50090-0836-1 20 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07630110/15/2008
Labeler - A-S Medication Solutions (830016429)
Establishment
NameAddressID/FEIOperations
A-S Medication Solutions830016429RELABEL(50090-0836), REPACK(50090-0836)

 
A-S Medication Solutions

← See all Loratadine antihistamine brands

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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