# Loratadine

NDC: 51660-753
Generic name: Loratadine
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20180601

FDA application: ANDA210088

## Active ingredients

- LORATADINE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-753"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-753
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b83de07d-37f4-42b4-b43e-29173454bef0