# Loratadine

NDC: 30142-066
Generic name: Loratadine
Labeler / Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210315

FDA application: ANDA208314

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30142-066"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-066
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b96831f5-5e75-c526-e053-2995a90a36ad