FDA NDC Directory · JSON-LD · Markdown

All Day Allergy Relief

NDC 59726-915 · HUMAN OTC DRUG · TABLET

Generic nameLoratadine
Labeler / ManufacturerP & L Development, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075209
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20191030
Package count3

External sources

Source: openFDA. Public-domain (CC0).