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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71705-050
Application NumberNDA210867
Product Classification
M
Marketing Category
C73594
G
Generic Name
Moxidectin
Product Specifications
Route of AdministrationORAL
Effective DateNovember 30, 2023
FDA Product Classification
INGREDIENTS (1)
MOXIDECTINActive
Quantity: 2 mg in 1 1
Code: NGU5H31YO9
Classification: ACTIB