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"21695-715-30" National Drug Code (NDC)
Venlafaxine Hydrochloride 30 TABLET in 1 BOTTLE (21695-715-30)
(Rebel Distributors Corp.)
NDC Code
21695-715-30
Package Description
30 TABLET in 1 BOTTLE (21695-715-30)
Product NDC
21695-715
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Venlafaxine Hydrochloride
Non-Proprietary Name
Venlafaxine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090903
Marketing Category Name
ANDA
Application Number
ANDA076690
Manufacturer
Rebel Distributors Corp.
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/21695-715-30