# Allergy Relief

NDC: 57344-193
Generic name: Loratadine
Labeler / Manufacturer: AAA PHARMACEUTICAL, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200814

FDA application: ANDA210722

## 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:"57344-193"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57344-193
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c8535e3-6a60-4640-b37e-a2260936d9af