# Claritin

NDC: 85237-1630
Generic name: loratadine
Labeler / Manufacturer: Select Consumer Group
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201201

FDA application: ANDA075209

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85237-1630"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85237-1630
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3c9ad1f8-e8ef-bcd0-e063-6394a90ac20e