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"0093-7544-10" National Drug Code (NDC)
Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-7544-10)
(Teva Pharmaceuticals USA Inc)
NDC Code
0093-7544-10
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-7544-10)
Product NDC
0093-7544
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20131211
Marketing Category Name
ANDA
Application Number
ANDA090783
Manufacturer
Teva Pharmaceuticals USA Inc
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
60
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/0093-7544-10