# Loratadine

NDC: 30142-565
Generic name: Loratadine
Labeler / Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20240315

FDA application: ANDA210088

## Active ingredients

- LORATADINE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30142-565"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-565
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=087ee83f-71aa-3d47-e063-6394a90aed4d