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"64725-1100-1" National Drug Code (NDC)
Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (64725-1100-1)
(TYA Pharmaceuticals)
NDC Code
64725-1100-1
Package Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (64725-1100-1)
Product NDC
64725-1100
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine Hydrochloride
Non-Proprietary Name
Duloxetin Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20131211
Marketing Category Name
ANDA
Application Number
ANDA090774
Manufacturer
TYA Pharmaceuticals
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/64725-1100-1