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Loperamide Hydrochloride

NDC 73581-175 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerYYBA CORP
Marketing categoryAbbreviated NDA (generic) · App ANDA206548
Dosage form / routeTABLET · ORAL
Active ingredientsLOPERAMIDE HYDROCHLORIDE (2 mg/1)
Marketing started20260713
Package count1

External sources

Source: openFDA. Public-domain (CC0).