# Loratadine

NDC: 80513-711
Generic name: Loratadine
Labeler / Manufacturer: Advanced Rx LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200101

FDA application: ANDA210722

## 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:"80513-711"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80513-711
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e96b4671-82dc-4cc6-a8bf-ef6f1efd8a7d