# Loratadine

NDC: 54838-554
Generic name: Loratadine
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20101124

FDA application: ANDA077421

## Active ingredients

- LORATADINE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54838-554"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54838-554
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=069c4e75-1f9f-4ab5-9570-3d93d12c2a23