"65862-407-99" National Drug Code (NDC)

Venlafaxine 1000 TABLET in 1 BOTTLE (65862-407-99)
(Aurobindo Pharma Limited)

NDC Code65862-407-99
Package Description1000 TABLET in 1 BOTTLE (65862-407-99)
Product NDC65862-407
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20100407
Marketing Category NameANDA
Application NumberANDA090555
ManufacturerAurobindo Pharma Limited
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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