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

"70710-1348-1" National Drug Code (NDC)

Venlafaxine 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-1)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1348-1
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-1)
Product NDC70710-1348
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
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/70710-1348-1





Copyright © 2007-2024 www.ndcvalidator.com