Lodosyn
LODOSYN (carbidopa) Tablets
Approved
Approval ID
ff8e105b-7415-42d4-bbb2-b36cfb8945a5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 1, 2020
Manufacturers
FDA
Bausch Health US, LLC
DUNS: 831922468
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
carbidopa
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code25010-711
Application NumberNDA017830
Product Classification
M
Marketing Category
C73594
G
Generic Name
carbidopa
Product Specifications
Route of AdministrationORAL
Effective DateJuly 1, 2020
FDA Product Classification
INGREDIENTS (5)
carbidopaActive
Quantity: 25 mg in 1 1
Code: MNX7R8C5VO
Classification: ACTIM
powdered celluloseInactive
Code: SMD1X3XO9M
Classification: IACT
FD&C Yellow No. 6Inactive
Code: H77VEI93A8
Classification: IACT
starch, cornInactive
Code: O8232NY3SJ
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT