MedPath
FDA Approval

BENZPHETAMINE HYDROCHLORIDE

December 18, 2017

HUMAN PRESCRIPTION DRUG LABEL

Benzphetamine(50 mg in 1 1)

Manufacturing Establishments (1)

H. J. Harkins Company Inc.

H. J. Harkins Company Inc.

147681894

Products (1)

BENZPHETAMINE HYDROCHLORIDE

76519-1154

ANDA090968

ANDA (C73584)

ORAL

December 18, 2017

FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8Class: IACT
POLYVINYL ALCOHOL, UNSPECIFIEDInactive
Code: 532B59J990Class: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOAClass: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30Class: IACT
CARNAUBA WAXInactive
Code: R12CBM0EIZClass: IACT
Code: 43DWT87QT7Class: ACTIBQuantity: 50 mg in 1 1
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2Class: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JPClass: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4Class: IACT
TALCInactive
Code: 7SEV7J4R1UClass: IACT
POLYETHYLENE GLYCOL 3350Inactive
Code: G2M7P15E5PClass: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5XClass: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61UClass: IACT
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