"72865-197-30" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-197-30)
(XLCare Pharmaceuticals, Inc.)

NDC Code72865-197-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-197-30)
Product NDC72865-197
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210226
Marketing Category NameANDA
Application NumberANDA214419
ManufacturerXLCare Pharmaceuticals, Inc.
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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