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Loratadine Allergy Relief

NDC 55289-728 · HUMAN OTC DRUG · TABLET

Generic nameLoratadine
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076134
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20171101
Package count4

External sources

Source: openFDA. Public-domain (CC0).