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"67877-265-10" National Drug Code (NDC)
Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-10)
(Ascend Laboratories, LLC)
NDC Code
67877-265-10
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-10)
Product NDC
67877-265
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20120501
Marketing Category Name
ANDA
Application Number
ANDA203197
Manufacturer
Ascend Laboratories, LLC
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/67877-265-10