Synanthic Bovine Dewormer
(oxfendazole oral suspension)
Approved
Approval ID
152cde64-ff22-4a3e-bb78-65e159dbe6b6
Product Type
OTC ANIMAL DRUG LABEL
Effective Date
May 1, 2025
Manufacturers
FDA
Boehringer Ingelheim Animal Health USA Inc.
DUNS: 007134091
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
oxfendazole
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0010-3832
Application NumberNADA140854
Product Classification
M
Marketing Category
C73593
G
Generic Name
oxfendazole
Product Specifications
Route of AdministrationORAL
Effective DateMay 1, 2025
FDA Product Classification
INGREDIENTS (1)
OXFENDAZOLEActive
Quantity: 225 mg in 1 mL
Code: OMP2H17F9E
Classification: ACTIB