FDA NDC Directory · JSON-LD · Markdown

Desloratadine

NDC 69339-194 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNatco Pharma USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDESLORATADINE (5 mg/1)
Marketing started20260401
Package count2

External sources

Source: openFDA. Public-domain (CC0).