"61919-482-60" National Drug Code (NDC)

Duloxetine Hydrochloride 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-482-60)
(DIRECT RX)

NDC Code61919-482-60
Package Description60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-482-60)
Product NDC61919-482
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA203088
ManufacturerDIRECT RX
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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