Liothyronine Sodium
Liothyronine Sodium Tablets, USP
Approved
Approval ID
4a8f7bf4-fa8f-4cde-9be2-11d5a4e6f07f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 9, 2014
Manufacturers
FDA
Aidarex Pharmaceuticals LLC
DUNS: 801503249
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Liothyronine Sodium
PRODUCT DETAILS
NDC Product Code33261-964
Application NumberANDA090097
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 9, 2014
Generic NameLiothyronine Sodium
INGREDIENTS (6)
LIOTHYRONINE SODIUMActive
Quantity: 5 ug in 1 1
Code: GCA9VV7D2N
Classification: ACTIM
CALCIUM SULFATEInactive
Code: WAT0DDB505
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT