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"61919-482-60" National Drug Code (NDC)
Duloxetine Hydrochloride 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-482-60)
(DIRECT RX)
NDC Code
61919-482-60
Package Description
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-482-60)
Product NDC
61919-482
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine Hydrochloride
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE PELLETS
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA203088
Manufacturer
DIRECT RX
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
30
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/61919-482-60