# Loratadine

NDC: 68001-449
Generic name: Loratadine Oral
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20200731

FDA application: ANDA208931

## 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:"68001-449"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-449
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ab820f80-b5fc-7896-e053-2995a90a4b1c