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Loratadine

NDC 80425-0352 · HUMAN OTC DRUG · TABLET

Generic nameloratadine
Labeler / ManufacturerAdvanced Rx Pharmacy of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214684
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20230731
Package count1

External sources

Source: openFDA. Public-domain (CC0).