FDA NDC Directory · JSON-LD · Markdown

Loratadine

NDC 72983-500 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerTenshi Kaizen Pvt Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA212795
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (5 mg/1)
Marketing started20210519
Package count1

External sources

Source: openFDA. Public-domain (CC0).