Moxidectin
MOXIDECTIN tablets, for oral use These highlights do not include all the information needed to use MOXIDECTIN safely and effectively. See full prescribing information for MOXIDECTIN . Initial U.S. Approval: 2018
Approved
Approval ID
6eb02ae9-9065-176f-e053-2991aa0ac891
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 30, 2023
Manufacturers
FDA
Medicines Development for Global Health
DUNS: 754191398
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Moxidectin
PRODUCT DETAILS
NDC Product Code71705-050
Application NumberNDA210867
Marketing CategoryC73594
Route of AdministrationORAL
Effective DateNovember 30, 2023
Generic NameMoxidectin
INGREDIENTS (1)
MOXIDECTINActive
Quantity: 2 mg in 1 1
Code: NGU5H31YO9
Classification: ACTIB