FDA NDC Directory · JSON-LD · Markdown

Loratadine Allergy Relief

NDC 10135-763 · HUMAN OTC DRUG · TABLET

Generic nameLoratadine
Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076134
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20221001
Package count3

External sources

Source: openFDA. Public-domain (CC0).