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"42292-019-20" National Drug Code (NDC)
Duloxetine 100 BLISTER PACK in 1 BOX, UNIT-DOSE (42292-019-20) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (42292-019-01)
(Mylan Institutional Inc.)
NDC Code
42292-019-20
Package Description
100 BLISTER PACK in 1 BOX, UNIT-DOSE (42292-019-20) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (42292-019-01)
Product NDC
42292-019
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20161208
Marketing Category Name
ANDA
Application Number
ANDA090778
Manufacturer
Mylan Institutional Inc.
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/42292-019-20