FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 68788-8282 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076601
Dosage form / routeSOLUTION · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (1 mg/mL)
Marketing started20231025
Package count1

External sources

Source: openFDA. Public-domain (CC0).