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"70771-1344-0" National Drug Code (NDC)
Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-0)
(Zydus Lifesciences Limited)
NDC Code
70771-1344-0
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-0)
Product NDC
70771-1344
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20140527
Marketing Category Name
ANDA
Application Number
ANDA090728
Manufacturer
Zydus Lifesciences Limited
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
20
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/70771-1344-0