"16714-311-03" National Drug Code (NDC)

Venlafaxine 1000 TABLET in 1 BOTTLE (16714-311-03)
(NorthStar RxLLC)

NDC Code16714-311-03
Package Description1000 TABLET in 1 BOTTLE (16714-311-03)
Product NDC16714-311
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20101221
Marketing Category NameANDA
Application NumberANDA078932
ManufacturerNorthStar RxLLC
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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