Probenecid
Probenecid Tablets USPRevised: June 2009Rx only 190811
Approved
Approval ID
5ca3dd4c-b8b4-4131-a066-214dabb2576f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 29, 2012
Manufacturers
FDA
HHS/Program Support Center/Supply Service Center
DUNS: 194032918
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Probenecid
PRODUCT DETAILS
NDC Product Code11819-282
Application NumberANDA084442
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateFebruary 29, 2012
Generic NameProbenecid
INGREDIENTS (13)
ProbenecidActive
Quantity: 500 mg in 1 1
Code: PO572Z7917
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
POLYETHYLENE GLYCOLSInactive
Code: 3WJQ0SDW1A
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT