# Allergy relief-D

NDC: 51660-940
Generic name: Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170502

FDA application: ANDA090922

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-940"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-940
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c24f3760-70e0-410f-bf80-6d0cadcd61b9