"75834-219-30" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-30)
(Nivagen Pharmaceuticals, Inc.)

NDC Code75834-219-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-30)
Product NDC75834-219
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190906
Marketing Category NameANDA
Application NumberANDA211323
ManufacturerNivagen Pharmaceuticals, Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength225
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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