Levothyroxine Sodium
Levothyroxine Sodium
Approved
Approval ID
7a5a9e87-383a-4450-bf79-1f4f68655ace
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 22, 2015
Manufacturers
FDA
Northwind Pharmaceuticals
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Levothyroxine Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-295
Application NumberNDA021342
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 23, 2015
FDA Product Classification
INGREDIENTS (1)
LEVOTHYROXINE SODIUMActive
Quantity: 0.1 mg in 1 1
Code: 9J765S329G
Classification: ACTIR