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"16714-312-03" National Drug Code (NDC)

Venlafaxine 1000 TABLET in 1 BOTTLE (16714-312-03)
(NorthStar RxLLC)

NDC Code16714-312-03
Package Description1000 TABLET in 1 BOTTLE (16714-312-03)
Product NDC16714-312
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
Strength37.5
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-312-03





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