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"16714-655-01" National Drug Code (NDC)
Venlafaxine 100 TABLET in 1 BOTTLE (16714-655-01)
(Northstar Rx LLC)
NDC Code
16714-655-01
Package Description
100 TABLET in 1 BOTTLE (16714-655-01)
Product NDC
16714-655
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine
Non-Proprietary Name
Venlafaxine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170126
End Marketing Date
20240930
Marketing Category Name
ANDA
Application Number
ANDA078627
Manufacturer
Northstar Rx LLC
Substance Name
VENLAFAXINE HYDROCHLORIDE
Strength
25
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/16714-655-01