# Loratadine

NDC: 63548-0753
Generic name: Loratadine
Labeler / Manufacturer: PLD Acquisitions LLC DBA Avma Pharma Solutions
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181030

FDA application: ANDA075209

## Active ingredients

- LORATADINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63548-0753"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63548-0753
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2edb53f8-7661-4e54-bb50-e03078bae3bf