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Loperamide hydrochloride

NDC 70771-1769 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA217471
Dosage form / routeCAPSULE · ORAL
Active ingredientsLOPERAMIDE HYDROCHLORIDE (2 mg/1)
Marketing started20230625
Package count3

External sources

Source: openFDA. Public-domain (CC0).