LORATADINE ANTIHISTAMINE- loratadine tablet 
Preferred Pharmaceuticals Inc.

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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

Principal Display Panel

Compare to Claritin® active ingredient

Original Prescription Strength

Non-Drowsy*

Loratadine Tablets, 10 mg

Antihistamine

Indoor & Outdoor Allergies

24 Hour Relief of:

Repackaged By: Preferred Pharmaceuticals Inc.

• Sneezing

• Runny Nose

• Itchy, Watery Eyes

• Itchy Throat or Nose

*When taken as directed. See Drug Facts Panel.

actual size

Padagis

Repackaged By: Preferred Pharmaceuticals Inc.

Loratadine Tablets 10mg
LORATADINE  ANTIHISTAMINE
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-8629(NDC:45802-650)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize8mm
FlavorImprint Code L612
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68788-8629-010 in 1 BOTTLE; Type 0: Not a Combination Product04/11/2024
2NDC:68788-8629-114 in 1 BOTTLE; Type 0: Not a Combination Product04/11/2024
3NDC:68788-8629-515 in 1 BOTTLE; Type 0: Not a Combination Product04/11/2024
4NDC:68788-8629-330 in 1 BOTTLE; Type 0: Not a Combination Product04/11/2024
5NDC:68788-8629-990 in 1 BOTTLE; Type 0: Not a Combination Product04/11/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07630104/11/2024
Labeler - Preferred Pharmaceuticals Inc. (791119022)
Registrant - Preferred Pharmaceuticals Inc. (791119022)
Establishment
NameAddressID/FEIBusiness Operations
Preferred Pharmaceuticals Inc.791119022REPACK(68788-8629)

Revised: 4/2024
Document Id: c5ea59d1-da03-4552-9db5-b90216988891
Set id: c5ea59d1-da03-4552-9db5-b90216988891
Version: 1
Effective Time: 20240411
 
Preferred Pharmaceuticals Inc.