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"68071-2139-3" National Drug Code (NDC)

Venlafaxine 30 TABLET in 1 BOTTLE (68071-2139-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2139-3
Package Description30 TABLET in 1 BOTTLE (68071-2139-3)
Product NDC68071-2139
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20080613
Marketing Category NameANDA
Application NumberANDA078627
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength50
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/68071-2139-3





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