# Loratadine and Pseudoephedrine Sulfate

NDC: 37808-724
Generic name: loratadine and pseudoephedrine sulfate
Labeler / Manufacturer: HEB
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180201

FDA application: ANDA076557

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-724"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-724
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74e7670a-5eca-4556-a860-0d36e8561518