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"49349-089-02" National Drug Code (NDC)
Venlafaxine Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-089-02)
(REMEDYREPACK INC.)
NDC Code
49349-089-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-089-02)
Product NDC
49349-089
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine Hydrochloride
Non-Proprietary Name
Venlafaxine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20101123
Marketing Category Name
ANDA
Application Number
ANDA077653
Manufacturer
REMEDYREPACK INC.
Substance Name
VENLAFAXINE HYDROCHLORIDE
Strength
37.5
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/49349-089-02