"68001-497-04" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-497-04)
(BluePoint Laboratories)

NDC Code68001-497-04
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-497-04)
Product NDC68001-497
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210430
Marketing Category NameANDA
Application NumberANDA214419
ManufacturerBluePoint Laboratories
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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