# allergy relief d

NDC: 37808-651
Generic name: cetirizine hydrochloride, pseudoephedrine hydrochloride
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210218

FDA application: ANDA210719

## 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:"37808-651"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-651
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b3ca8aae-04f2-4c00-9fb5-ce3ed7e6f1bb