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"71335-0778-3" National Drug Code (NDC)

Venlafaxine 90 TABLET in 1 BOTTLE (71335-0778-3)
(Bryant Ranch Prepack)

NDC Code71335-0778-3
Package Description90 TABLET in 1 BOTTLE (71335-0778-3)
Product NDC71335-0778
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20151001
Marketing Category NameANDA
Application NumberANDA078932
ManufacturerBryant Ranch Prepack
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength75
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0778-3





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