# Loratadine

NDC: 68071-2392
Generic name: Loratadine
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200201

FDA application: ANDA075209

## 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:"68071-2392"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2392
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c0e3057d-2dd2-de2b-e053-2995a90a1a1d