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"61919-042-30" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-042-30)
(DIRECT RX)

NDC Code61919-042-30
Package Description30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-042-30)
Product NDC61919-042
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
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/61919-042-30





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