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"60505-2996-8" National Drug Code (NDC)
Duloxetine Hydrochloride 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-2996-8)
(Apotex Corp.)
NDC Code
60505-2996-8
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-2996-8)
Product NDC
60505-2996
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine Hydrochloride
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20140613
Marketing Category Name
ANDA
Application Number
ANDA202045
Manufacturer
Apotex Corp.
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
30
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/60505-2996-8