FDA NDC Directory · JSON-LD · Markdown

Loratadine

NDC 68016-053 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerPremier Value
Marketing categoryAbbreviated NDA (generic) · App ANDA210088
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (5 mg/1)
Marketing started20180401
Package count2

External sources

Source: openFDA. Public-domain (CC0).