www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"69097-299-15" National Drug Code (NDC)
Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69097-299-15)
(Cipla USA Inc.)
NDC Code
69097-299-15
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69097-299-15)
Product NDC
69097-299
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20151205
Marketing Category Name
ANDA
Application Number
ANDA202336
Manufacturer
Cipla 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/69097-299-15