# Loratadine antihistamine

NDC: 72789-347
Generic name: Loratadine
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20081015

FDA application: ANDA076301

## 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:"72789-347"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-347
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=039f144b-891b-4ab0-e063-6394a90aa4c8