"57664-395-88" National Drug Code (NDC)

Venlafaxine 100 TABLET in 1 BOTTLE (57664-395-88)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-395-88
Package Description100 TABLET in 1 BOTTLE (57664-395-88)
Product NDC57664-395
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20080613
Marketing Category NameANDA
Application NumberANDA078627
ManufacturerSun Pharmaceutical Industries, Inc.
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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