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Cetirizine Hydrochloride

NDC 49483-682 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerTIME CAP LABORATORIES, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078933
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
Marketing started20220530
Package count1

External sources

Source: openFDA. Public-domain (CC0).