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Loperamide Hydrochloride

NDC 68016-123 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerChain Drug Consortium, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074091
Dosage form / routeTABLET · ORAL
Active ingredientsLOPERAMIDE HYDROCHLORIDE (2 mg/1)
Marketing started19930201
Package count4

External sources

Source: openFDA. Public-domain (CC0).