# Loratadine and Pseudoephedrine

NDC: 51660-724
Generic name: loratadine and pseudoephedrine
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20041117

FDA application: ANDA076557

## Active ingredients

- LORATADINE: 10 mg/1
- PSEUDOEPHEDRINE SULFATE: 240 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-724"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-724
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=556b89ef-3b51-4faa-afb4-767a5c1b6422