# Loratadine ODT

NDC: 49035-806
Generic name: Loratadine
Labeler / Manufacturer: Wal-Mart Stores, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20180411

FDA application: ANDA208477

## 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:"49035-806"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49035-806
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7679ee14-08aa-459c-9107-1a7144379962