"13811-712-30" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-712-30)
(Trigen Laboratories, LLC)

NDC Code13811-712-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-712-30)
Product NDC13811-712
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20100429
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022104
ManufacturerTrigen Laboratories, LLC
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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