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"61786-419-02" National Drug Code (NDC)
Venlafaxine 30 TABLET in 1 BLISTER PACK (61786-419-02)
(REMEDYREPACK INC.)
NDC Code
61786-419-02
Package Description
30 TABLET in 1 BLISTER PACK (61786-419-02)
Product NDC
61786-419
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine
Non-Proprietary Name
Venlafaxine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150926
Marketing Category Name
ANDA
Application Number
ANDA078627
Manufacturer
REMEDYREPACK INC.
Substance Name
VENLAFAXINE HYDROCHLORIDE
Strength
75
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/61786-419-02