# non drowsy allergy relief

NDC: 41250-890
Generic name: loratadine
Labeler / Manufacturer: Meijer Distribution Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20200923

FDA application: ANDA076011

## 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:"41250-890"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41250-890
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4762c96e-d562-4f74-a275-8cba597987f9