# UP AND UP CHILDRENS ALLERGY

NDC: 82442-207
Generic name: Loratadine
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20240731

FDA application: ANDA075728

## Active ingredients

- LORATADINE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82442-207"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82442-207
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a9f6ae02-cf29-4111-99e7-7e6b1ecb88f0