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Levocetirizine Dihydrochloride

NDC 42571-312 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211551
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20190201
Package count4

External sources

Source: openFDA. Public-domain (CC0).