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"68382-019-16" National Drug Code (NDC)

Venlafaxine 90 TABLET in 1 BOTTLE (68382-019-16)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-019-16
Package Description90 TABLET in 1 BOTTLE (68382-019-16)
Product NDC68382-019
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20080613
Marketing Category NameANDA
Application NumberANDA077653
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength37.5
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/68382-019-16





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