"61919-351-60" National Drug Code (NDC)

Venlafaxine 60 TABLET in 1 BOTTLE (61919-351-60)
(Direct_Rx)

NDC Code61919-351-60
Package Description60 TABLET in 1 BOTTLE (61919-351-60)
Product NDC61919-351
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20171031
Marketing Category NameANDA
Application NumberANDA202036
ManufacturerDirect_Rx
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength75
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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