"71205-602-90" National Drug Code (NDC)

Duloxetine 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)
(Proficient Rx LP)

NDC Code71205-602-90
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)
Product NDC71205-602
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20170316
Marketing Category NameANDA
Application NumberANDA208706
ManufacturerProficient Rx LP
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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