# Loratadine

NDC: 63868-151
Generic name: Loratadine
Labeler / Manufacturer: Chain Drug Marketing Association Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20030819

FDA application: ANDA076134

## 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:"63868-151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4edf5b1-398d-405a-8a42-76044b31ebb7