# Loratadine

NDC: 30142-996
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: 20190522

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:"30142-996"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-996
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f7f7005-22db-4b88-9771-e31c21e9b2b1