# Loratadine ODT

NDC: 58602-821
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-821"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-821
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f44382f-c289-402d-bb98-ec5fa80fc25d