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Ivermectin

NDC 70771-1731 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216863
Dosage form / routeTABLET · ORAL
Active ingredientsIVERMECTIN (3 mg/1)
Marketing started20260227
Package count1

External sources

Source: openFDA. Public-domain (CC0).