"49349-089-02" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-089-02)
(REMEDYREPACK INC.)

NDC Code49349-089-02
Package Description30 TABLET in 1 BLISTER PACK (49349-089-02)
Product NDC49349-089
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20101123
Marketing Category NameANDA
Application NumberANDA077653
ManufacturerREMEDYREPACK INC.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength37.5
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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