# Loratadine Allergy Relief

NDC: 76420-330
Generic name: Loratadine
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171101

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:"76420-330"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-330
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=332bda00-1350-2d33-e063-6394a90a8bd7