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"70771-1652-3" National Drug Code (NDC)

Venlafaxine 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-3)
(Zydus Lifesciences Limited)

NDC Code70771-1652-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-3)
Product NDC70771-1652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220901
Marketing Category NameANDA
Application NumberANDA215622
ManufacturerZydus Lifesciences Limited
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength225
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/70771-1652-3





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