# Loratadine

NDC: 43598-756
Generic name: Loratadine
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210519

FDA application: ANDA212795

## 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:"43598-756"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-756
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9357186a-9452-e139-01d8-6b8c6f6a2c6b