FDA NDC Directory · JSON-LD · Markdown

Desloratadine

NDC 69452-363 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078357
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDESLORATADINE (5 mg/1)
Marketing started20231128
Package count2

External sources

Source: openFDA. Public-domain (CC0).