# Loratadine

NDC: 80425-0352
Generic name: loratadine
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230731

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:"80425-0352"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0352
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=01cb43cf-57a9-f189-e063-6294a90afd88