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"16714-420-06" National Drug Code (NDC)
Duloxetine Hydrochloride 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-420-06)
(NorthStar RxLLC)
NDC Code
16714-420-06
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-420-06)
Product NDC
16714-420
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine Hydrochloride
Proprietary Name Suffix
20 Mg
Non-Proprietary Name
Duloxetine
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20140609
Marketing Category Name
ANDA
Application Number
ANDA202949
Manufacturer
NorthStar RxLLC
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
20
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/16714-420-06