# Allergy Relief

NDC: 11822-3276
Generic name: Loratadine
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191227
Marketing ended: 20261227
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:"11822-3276"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-3276
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4cf4235-f76b-46da-bcf8-00d2d5f4d8ab