# cetirizine hydrochloride

NDC: 70677-1007
Generic name: Cetirizine Hydrochloride Tablets
Labeler / Manufacturer: Strategic Sourcing Services LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220512
Marketing ended: 20270228
FDA application: ANDA078343

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70677-1007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70677-1007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52b70885-f623-b1c8-29c6-584bff46ed45