# LORATADINE

NDC: 72983-501
Generic name: LORATADINE
Labeler / Manufacturer: Tenshi Kaizen Pvt Ltd
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20210519

FDA application: ANDA213294

## 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:"72983-501"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72983-501
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c20b916d-7dd0-1a56-e053-2995a90a3c1b