# Loratadine

NDC: 68001-438
Generic name: Loratadine
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200826

FDA application: ANDA208314

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-438"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-438
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=adc506ed-7a7a-facc-e053-2a95a90ae147