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Moxidectin

NDC 71705-050 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMedicines Development for Global Health
Marketing categoryNew Drug Application (innovator) · App NDA210867
Dosage form / routeTABLET · ORAL
Active ingredientsMOXIDECTIN (2 mg/1)
Marketing started20191202
Package count1

External sources

Source: openFDA. Public-domain (CC0).