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Loratadine

NDC 68210-4110 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerSpirit Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210722
Dosage form / routeTABLET · ORAL
Active ingredientsLORATADINE (10 mg/1)
Marketing started20200911
Package count1

External sources

Source: openFDA. Public-domain (CC0).