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"70710-1537-0" National Drug Code (NDC)

Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1537-0)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1537-0
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1537-0)
Product NDC70710-1537
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140527
Marketing Category NameANDA
Application NumberANDA090728
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesNorepinephrine 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/70710-1537-0





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