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"52125-868-02" National Drug Code (NDC)
Venlafaxine Hydrochloride 30 TABLET in 1 BLISTER PACK (52125-868-02)
(REMEDYREPACK INC.)
NDC Code
52125-868-02
Package Description
30 TABLET in 1 BLISTER PACK (52125-868-02)
Product NDC
52125-868
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine Hydrochloride
Non-Proprietary Name
Venlafaxine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140313
Marketing Category Name
ANDA
Application Number
ANDA079098
Manufacturer
REMEDYREPACK INC.
Substance Name
VENLAFAXINE HYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-868-02