# Allergy Relief D

NDC: 0363-2010
Generic name: loratadine, pseudoephedrine sulfate
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240207

FDA application: ANDA075989

## Active ingredients

- LORATADINE: 10 mg/1
- PSEUDOEPHEDRINE SULFATE: 240 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-2010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-2010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9952e0fb-b20e-4f9c-8be7-aa286e271fee