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Cetirizine hydrochloride

NDC 62207-764 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerGranules India Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA209274
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20180528
Package count3

External sources

Source: openFDA. Public-domain (CC0).