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"59651-279-71" National Drug Code (NDC)
Duloxetine 7000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-71)
(Aurobindo Pharma Limited)
NDC Code
59651-279-71
Package Description
7000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-71)
Product NDC
59651-279
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20131211
Marketing Category Name
ANDA
Application Number
ANDA090778
Manufacturer
Aurobindo Pharma Limited
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59651-279-71