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"57664-395-88" National Drug Code (NDC)
Venlafaxine 100 TABLET in 1 BOTTLE (57664-395-88)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-395-88
Package Description
100 TABLET in 1 BOTTLE (57664-395-88)
Product NDC
57664-395
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine
Non-Proprietary Name
Venlafaxine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20080613
Marketing Category Name
ANDA
Application Number
ANDA078627
Manufacturer
Sun Pharmaceutical Industries, Inc.
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/57664-395-88