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"52125-621-02" National Drug Code (NDC)

Venlafaxine 30 TABLET in 1 BLISTER PACK (52125-621-02)
(REMEDYREPACK INC.)

NDC Code52125-621-02
Package Description30 TABLET in 1 BLISTER PACK (52125-621-02)
Product NDC52125-621
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20130529
Marketing Category NameANDA
Application NumberANDA079009
ManufacturerREMEDYREPACK INC.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength75
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/52125-621-02





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