"16714-656-01" National Drug Code (NDC)

Venlafaxine 100 TABLET in 1 BOTTLE (16714-656-01)
(Northstar Rx LLC)

NDC Code16714-656-01
Package Description100 TABLET in 1 BOTTLE (16714-656-01)
Product NDC16714-656
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20170126
End Marketing Date20240930
Marketing Category NameANDA
Application NumberANDA078627
ManufacturerNorthstar Rx LLC
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength37.5
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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