# Loratadine

NDC: 62207-787
Generic name: Loratadine
Labeler / Manufacturer: Granules India Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200108

FDA application: ANDA210722

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62207-787"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62207-787
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9bae1ba3-c0da-23a2-e053-2a95a90a58ed