# Loratadine Allergy Relief

NDC: 55289-728
Generic name: Loratadine
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171101

FDA application: ANDA076134

## 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:"55289-728"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-728
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7127b39d-3686-4249-b720-43c02b4c4654