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Loratadine | Loratadine [Northwind Pharmaceuticals, LLC] | BioPortfolio

13:45 EST 27th January 2019 | BioPortfolio

Note: While we endeavour to keep our records up-to-date one should not rely on these details being accurate without first consulting a professional. Click here to read our full medical disclaimer.

Antihistamine

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

runny noseitchy, watery eyessneezingitching of the nose or throat

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.

Call 1-800-406-7984

NDC: 51655-027-26

MFG: 51660-526-05

Loratadine 10 MG

90 Tablets

Rx Only

Lot#

Exp. Date:

Medication guide is found at www.fda.gov/drugs/drugsafety/ucm085729

Dosage: See prescriber's instructions

Each tablet contains 10 mg of loratadine

Store at 68 to 77 degrees F.

Protect from light and moisture

Keep out of the reach of children.

Mfg. by Ohm Laboratories, North Brunswick, NJ 08902 Lot#

Repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46256

Manufacturer

Northwind Pharmaceuticals, LLC

Active Ingredients

Source

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Clinical Trials [37 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...

Loratadine for Improvement of Bone Pain in Patients With Chronic Granulocyte-Colony Stimulating Factor (G-CSF) Use

G-CSF causes a release of histamine that may be a cause of chronic bone pain. Loratadine targets histamine, and so may be effective in reducing bone pain.The researchers plan to prospectiv...

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...

PubMed Articles [3 Associated PubMed Articles listed on BioPortfolio]

Oral loratadine in the management of G-CSF-induced bone pain: a pilot study.

This pilot study aimed to ascertain if bone pain induced by granulocyte-colony stimulating factors (G-CSFs) can be alleviated or eliminated by oral antihistamine loratadine. Twelve patients with cance...

Inhibiting Surface Crystallization and Improving Dissolution of Amorphous Loratadine by Dextran Sulfate Nano-coating.

Amorphous formulations provide a solution to poor solubility and slow dissolution of many drugs, but fast surface crystallization can negate their advantages. As in the case of many amorphous drugs, l...

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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