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Products (1)

NDC Product Code

61958-1201

Application Number

NDA203100

Marketing Category

NDA (C73594)

Route of Administration

ORAL

Effective Date

September 16, 2021

Ingredients

LACTOSE MONOHYDRATEInactive

Code: EWQ57Q8I5XClass: IACT

TITANIUM DIOXIDEInactive

Code: 15FIX9V2JPClass: IACT

ElvitegravirActive

Code: 4GDQ854U53Class: ACTIBQuantity: 150 mg in 1 1

HYDROXYPROPYL CELLULOSE (1600000 WAMW)Inactive

Code: RFW2ET671PClass: IACT

POLYETHYLENE GLYCOL, UNSPECIFIEDInactive

Code: 3WJQ0SDW1AClass: IACT

POLYVINYL ALCOHOL, UNSPECIFIEDInactive

Code: 532B59J990Class: IACT

TALCInactive

Code: 7SEV7J4R1UClass: IACT

FD&C BLUE NO. 2Inactive

Code: L06K8R7DQKClass: IACT

ALUMINUM OXIDEInactive

Code: LMI26O6933Class: IACT

CobicistatActive

Code: LW2E03M5PGClass: ACTIBQuantity: 150 mg in 1 1

EmtricitabineActive

Code: G70B4ETF4SClass: ACTIBQuantity: 200 mg in 1 1

Tenofovir disoproxilActive

Code: OTT9J7900IClass: ACTIBQuantity: 300 mg in 1 1

MICROCRYSTALLINE CELLULOSEInactive

Code: OP1R32D61UClass: IACT

MAGNESIUM STEARATEInactive

Code: 70097M6I30Class: IACT

CROSCARMELLOSE SODIUMInactive

Code: M28OL1HH48Class: IACT

SILICON DIOXIDEInactive

Code: ETJ7Z6XBU4Class: IACT

SODIUM LAURYL SULFATEInactive

Code: 368GB5141JClass: IACT

FERRIC OXIDE YELLOWInactive

Code: EX438O2MRTClass: IACT

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