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"61919-351-60" National Drug Code (NDC)
Venlafaxine 60 TABLET in 1 BOTTLE (61919-351-60)
(Direct_Rx)
NDC Code
61919-351-60
Package Description
60 TABLET in 1 BOTTLE (61919-351-60)
Product NDC
61919-351
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine
Non-Proprietary Name
Venlafaxine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20171031
Marketing Category Name
ANDA
Application Number
ANDA202036
Manufacturer
Direct_Rx
Substance Name
VENLAFAXINE HYDROCHLORIDE
Strength
75
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine 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/61919-351-60