# Loratadine

NDC: 69848-019
Generic name: Loratadine
Labeler / Manufacturer: GRANULES USA, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210726

FDA application: ANDA210722

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69848-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69848-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c3c9bc45-7ed5-abf4-e053-2995a90a40ff