Drug Facts | Loratadine

12:42 EDT 24th July 2014 | BioPortfolio

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Loratadine, USP 10 mg


Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

They are supplied by State of Florida DOH Central Pharmacy as follows:

NDC Strength Quantity/Form Color Source Prod. Code
53808-0457-1 10 mg 30 Tablets in a Blister Pack WHITE 45802-0650

if you have ever had an allergic reaction to this product or any of its ingredients.

liver or kidney disease.Your doctor should determine if you need a different dose.

do not take more than directed. Taking more than directed may cause drowsiness.

if an allergic reaction to this product occurs. Seek medical help right away.

ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

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

Lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.

1 800 719-9260

This product is manufactured by:

Perrigo Company515 Eastern Avenue AlleganMichigan 49010

This Product was Repackaged By:

State of Florida DOH Central Pharmacy 104-2 Hamilton Park Drive Tallahassee, FL 32304 United States

NDC 53808-0457-1 Non-Drowsy*


Tablets, USP

10 mg


Indoor & Outdoor Allergies

24 Hour

Relief of:

• Sneezing

• Runny Nose

• Itchy, Watery


• Itchy Throat

or Nose

* When taken as directed.

See Drug Facts Panel.

IMAGE Loratadine 10mg(Perrigo).jpg


State of Florida DOH Central Pharmacy

Active Ingredients


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Drug Facts

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Non-Drowsy* Claritin loratadine tablets 10 mg/antihistamine

Clinical Trials [35 Associated Clinical Trials listed on BioPortfolio]

Post Approval Pharmacokinetic Study of Loratadine in Japanese Pediatric and Adult Patients (Study P05539)(COMPLETED)

This is a post marketing study to confirm the appropriate dose of loratadine in children by obtaining drug concentration data at multiple time points per child and adult patient, after the...

Bioequivalence Study on Loratadine Orally Disintegrating Tablets 10 mg Under Fasting Conditions

To compare the single-dose oral bioavailability of loratadine 10 mg orally disintegrating tablets of Ohm Laboratories (a subsidiary of Ranbaxy Pharmaceuticals Inc., USA) with Claritin® Re...

To Demonstrate the Relative Bioavailability Study of Loratadine 10 mg Tablets

To demonstrate the relative bioavailability study of Loratadine 10 mg tablets.

Efficacy and Adverse Effects of Prapchompoothaweep Remedy and Loratadine for Treatment in AR Patients

1. To compare the effectiveness of Prapchompoothaweep crude drug at 3,000 mg per day and Loratadine 10 mg per day for treatment in Allergic Rhinitis patients. (Clinical Trial Pha...

Benjakul Extract and Loratadine for Treatment Allergic Rhinitis Patients

1. To compare the effectiveness of Benjakul extract capsules at 300 mg per day with Loratadine drug in the treatment of allergic rhinitis patients in small group (Clinical Trial ...

PubMed Articles [5 Associated PubMed Articles listed on BioPortfolio]

Qingfeijianpi therapy for persistent allergic rhinitis: A randomized, positive-controlled clinical trial.

This study aims to investigate the effectiveness and safety of Qingfeijianpi therapy for persistent allergic rhinitis (AR).A total of 101 patients with persistent AR were included into the study. Thes...

Design and characterization of loratadine nanosuspension prepared by ultrasonic-assisted precipitation.

Nanoparticle engineering is a well-defined technique employed as a novel and effective method in drug design and delivery. It is widely used to control particle size, as well as the morphological and ...

Combination therapy with montelukast and loratadine alleviates pharyngo-laryngeal symptoms related to seasonal allergic rhinitis.

Effect of taste masking technology on fast dissolving oral film: Dissolution rate and bioavailability.

Fast dissolving oral film is a stamp-style drug loaded polymer film with rapid disintegration and dissolution. This new kind of drug delivery system has harsh requirements on the taste-masking technol...

Automated morphological feature assessment for zebrafish embryo developmental toxicity screens.

Detection of developmental phenotypes in zebrafish embryos typically involves a visual assessment and scoring of morphological features by an individual researcher. Subjective scoring could impact res...

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