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"70771-1346-0" National Drug Code (NDC)

Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1346-0)
(Zydus Lifesciences Limited)

NDC Code70771-1346-0
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1346-0)
Product NDC70771-1346
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140527
Marketing Category NameANDA
Application NumberANDA090728
ManufacturerZydus Lifesciences Limited
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
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/70771-1346-0





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