FDA NDC Directory · JSON-LD · Markdown

Loratadine

NDC 68788-8659 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210722
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20240513
Package count5

External sources

Source: openFDA. Public-domain (CC0).