FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 43598-183 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride Tablets
Labeler / ManufacturerDr. Reddy's Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078343
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20181217
Package count2

External sources

Source: openFDA. Public-domain (CC0).