"61919-617-30" National Drug Code (NDC)

Venlafaxine 30 TABLET in 1 BOTTLE (61919-617-30)
(DIRECT RX)

NDC Code61919-617-30
Package Description30 TABLET in 1 BOTTLE (61919-617-30)
Product NDC61919-617
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20190424
Marketing Category NameANDA
Application NumberANDA078932
ManufacturerDIRECT RX
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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