# Childrens Loratadine

NDC: 51672-2085
Generic name: Loratadine
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20040820

FDA application: ANDA076805

## 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:"51672-2085"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2085
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12c8066a-3429-481e-b63a-7ea2b439a170