Drugplain

Loratadine ODT 10 mg/1

Loratadine · TABLET, ORALLY DISINTEGRATING · Aurohealth LLC

No Recall History
Plain English

Loratadine ODT is a tablet, orally disintegrating containing loratadine at 10 mg/1, taken oral. Manufactured by Aurohealth LLC.

Key Facts

Brand Name
Loratadine ODT
Generic Name
Loratadine
NDC Code (Product)
58602-821
Manufacturer
Aurohealth LLC
Strength
10 mg/1
Dosage Form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Marketing Status
Application #
ANDA208477
Marketing Start
04/11/2018

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective3,548 reports
fatigue3,226 reports
nausea2,698 reports
dyspnoea2,432 reports
headache2,406 reports
diarrhoea2,366 reports
off label use2,229 reports
dizziness2,066 reports
pain1,979 reports
rash1,618 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Dosage & Administration

Directions place 1 tablet on tongue; tablet disintegrates, with or without water 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

Warnings

Warnings

Frequently Asked Questions

What is Loratadine ODT used for?

Loratadine ODT contains Loratadine. It is a tablet, orally disintegrating taken oral. Consult your doctor for specific uses.

Is Loratadine ODT a controlled substance?

Loratadine ODT is not classified as a controlled substance by the DEA.

What is the generic name for Loratadine ODT?

The generic name for Loratadine ODT is Loratadine. There are 12 other brand versions of Loratadine.

What is the NDC code for Loratadine ODT 10 mg/1?

The NDC (National Drug Code) for Loratadine ODT 10 mg/1 is 58602-821, listed by Aurohealth LLC.

Product NDC

58602-821

Package NDC

58602-821-83

Other Loratadine Brands

See all →

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)