# Loratadine ODT

NDC: 58602-744
Generic name: Loratadine
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20180411

FDA application: ANDA208477

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-744"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-744
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8c119b12-f512-4207-b354-7244d1f9963a