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"70518-2114-0" National Drug Code (NDC)

Venlafaxine 30 TABLET in 1 BLISTER PACK (70518-2114-0)
(REMEDYREPACK INC.)

NDC Code70518-2114-0
Package Description30 TABLET in 1 BLISTER PACK (70518-2114-0)
Product NDC70518-2114
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20190523
Marketing Category NameANDA
Application NumberANDA078627
ManufacturerREMEDYREPACK INC.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2114-0





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