FDA NDC Directory · JSON-LD · Markdown

Allergy

NDC 63654-309 · HUMAN OTC DRUG · TABLET

Generic nameLoratadine
Labeler / ManufacturerSelder, S.A. de C.V.
Marketing categoryAbbreviated NDA (generic) · App ANDA076471
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20141216
Package count1

External sources

Source: openFDA. Public-domain (CC0).