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Loratadine

NDC 16571-822 · HUMAN OTC DRUG · TABLET

Generic nameloratadine
Labeler / ManufacturerRising Pharmaceuticals, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA214684
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20220310
Package count3

External sources

Source: openFDA. Public-domain (CC0).