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Cetirizine hydrochloride

NDC 23155-929 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078876
Dosage form / routeSOLUTION · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/5mL)
Marketing started20250301
Package count2

External sources

Source: openFDA. Public-domain (CC0).