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"0002-3270-33" National Drug Code (NDC)
Cymbalta 100 BLISTER PACK in 1 CARTON (0002-3270-33) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0002-3270-01)
(Eli Lilly and Company)
NDC Code
0002-3270-33
Package Description
100 BLISTER PACK in 1 CARTON (0002-3270-33) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0002-3270-01)
Product NDC
0002-3270
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cymbalta
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20100115
Marketing Category Name
NDA
Application Number
NDA021427
Manufacturer
Eli Lilly and Company
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/0002-3270-33