# Loratadine Allergy Relief

NDC: 10135-763
Generic name: Loratadine
Labeler / Manufacturer: Marlex Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20221001

FDA application: ANDA076134

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10135-763"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10135-763
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ec08a6ee-3d71-0fa9-e053-2995a90a9cb1