MedPath
FDA Approval

Venlafaxine Hydrochloride

May 10, 2019

HUMAN PRESCRIPTION DRUG LABEL

Venlafaxine(37.5 mg in 1 1)

Manufacturing Establishments (1)

NuCare Pharmaceuticals,Inc.

NuCare Pharmaceuticals,Inc.

010632300

Products (1)

Venlafaxine Hydrochloride

68071-4250

ANDA076565

ANDA (C73584)

ORAL

May 10, 2019

FERROSOFERRIC OXIDEInactive
Code: XM0M87F357Class: IACT
POLYETHYLENE GLYCOL 400Inactive
Code: B697894SGQClass: IACT
DIBUTYL SEBACATEInactive
Code: 4W5IH7FLNYClass: IACT
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327LClass: IACT
ETHYLCELLULOSE (7 MPA.S)Inactive
Code: H3UP11403CClass: IACT
SHELLACInactive
Code: 46N107B71OClass: IACT
SUCROSEInactive
Code: C151H8M554Class: IACT
TALCInactive
Code: 7SEV7J4R1UClass: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JPClass: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3GClass: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8Class: IACT
POTASSIUM HYDROXIDEInactive
Code: WZH3C48M4TClass: IACT
POVIDONE K30Inactive
Code: U725QWY32XClass: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3Class: IACT
STARCH, CORNInactive
Code: O8232NY3SJClass: IACT
Code: 7D7RX5A8MOClass: ACTIMQuantity: 37.5 mg in 1 1
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