# Allergy Relief

NDC: 51660-527
Generic name: Loratadine
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20070831

FDA application: ANDA077153

## 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:"51660-527"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-527
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de3a7725-5d1b-4195-a9f8-43f92888997c