# Loratadine Allergy Relief

NDC: 51660-526
Generic name: Loratadine
Labeler / Manufacturer: OHM LABORATORIES 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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-526"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-526
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c35f2cc1-f76d-4824-b0a5-747bca0c3b85