# Claritin

NDC: 70264-030
Generic name: Loratadine
Labeler / Manufacturer: R J General Corporation
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210301

FDA application: NDA019658

## 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:"70264-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70264-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a34e8cb7-4fdf-45be-b288-45d93eef6220