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Loperamide Hydrochloride and Simethicone

NDC 58602-815 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211059
Dosage form / routeTABLET · ORAL
Active ingredientsDIMETHICONE (125 mg/1)
LOPERAMIDE HYDROCHLORIDE (2 mg/1)
Marketing started20201214
Package count4

External sources

Source: openFDA. Public-domain (CC0).