# Loratadine

NDC: 82501-1580
Generic name: Loratadine
Labeler / Manufacturer: Gobrands, Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220516

FDA application: ANDA214684

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82501-1580"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82501-1580
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d182bd6-ad72-4352-b983-407a48c317f0