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"47335-747-18" National Drug Code (NDC)

Desvenlafaxine 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-747-18)
(Sun Pharma Global FZE)

NDC Code47335-747-18
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-747-18)
Product NDC47335-747
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDesvenlafaxine
Non-Proprietary NameDesvenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140130
Marketing Category NameNDA
Application NumberNDA205583
ManufacturerSun Pharma Global FZE
Substance NameDESVENLAFAXINE FUMARATE MONOHYDRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-747-18





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