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"47335-383-08" National Drug Code (NDC)
Duloxetine 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-08)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-383-08
Package Description
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-08)
Product NDC
47335-383
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
ANDA090745
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
60
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/47335-383-08