FDA NDC Directory · JSON-LD · Markdown

Loratadine antihistamine

NDC 72789-347 · HUMAN OTC DRUG · TABLET

Generic nameLoratadine
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076301
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20081015
Package count5

External sources

Source: openFDA. Public-domain (CC0).