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"71335-1212-1" National Drug Code (NDC)

Venlafaxine 30 TABLET in 1 BOTTLE (71335-1212-1)
(Bryant Ranch Prepack)

NDC Code71335-1212-1
Package Description30 TABLET in 1 BOTTLE (71335-1212-1)
Product NDC71335-1212
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20100407
Marketing Category NameANDA
Application NumberANDA090555
ManufacturerBryant Ranch Prepack
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength100
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/71335-1212-1





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