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"70710-1352-1" National Drug Code (NDC)

Venlafaxine 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-1)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1352-1
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-1)
Product NDC70710-1352
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220901
Marketing Category NameANDA
Application NumberANDA215622
ManufacturerZydus Pharmaceuticals USA Inc.
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/70710-1352-1





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