# Loratadine

NDC: 16571-822
Generic name: loratadine
Labeler / Manufacturer: Rising Pharmaceuticals, Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220310

FDA application: ANDA214684

## 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:"16571-822"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-822
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d28128a3-af54-440e-9bd4-0fccf393d18a