# Loratadine

NDC: 84386-119
Generic name: Loratadine
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20251112

FDA application: ANDA208314

## 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:"84386-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84386-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f4ffb72-f4e8-4617-8bc5-61e6de488a2d