# Loratadine Allergy Relief

NDC: 37808-529
Generic name: Loratadine
Labeler / Manufacturer: HEB
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180201

FDA application: ANDA076134

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-529"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-529
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6703e4f3-e9b8-4c70-9085-3d6ac0d7fbda