# Loratadine

NDC: 0363-9955
Generic name: Loratadine
Labeler / Manufacturer: Walgreens Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210519

FDA application: ANDA212795

## Active ingredients

- LORATADINE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-9955"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-9955
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8229ca40-31cf-3dbd-078d-364f5674cb21