Salsalate
Salsalate Tablets, USP500 mg and 750 mgRx Only
Approved
Approval ID
8bc31246-b962-46fd-b235-26c34b1b0781
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 27, 2023
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Salsalate
PRODUCT DETAILS
NDC Product Code63629-9248
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateAugust 10, 2020
Generic NameSalsalate
INGREDIENTS (9)
SODIUM STARCH GLYCOLATE TYPE AInactive
Code: H8AV0SQX4D
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
TRIACETINInactive
Code: XHX3C3X673
Classification: IACT
SALSALATEActive
Quantity: 500 mg in 1 1
Code: V9MO595C9I
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
HYPROMELLOSE, UNSPECIFIEDInactive
Code: 3NXW29V3WO
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT