www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"70771-1649-3" National Drug Code (NDC)

Venlafaxine 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1649-3)
(Zydus Lifesciences Limited)

NDC Code70771-1649-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1649-3)
Product NDC70771-1649
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
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/70771-1649-3





Copyright © 2007-2024 www.ndcvalidator.com