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"59651-282-39" National Drug Code (NDC)

Duloxetine 3000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-282-39)
(Aurobindo Pharma Limited)

NDC Code59651-282-39
Package Description3000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-282-39)
Product NDC59651-282
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131211
Marketing Category NameANDA
Application NumberANDA090778
ManufacturerAurobindo Pharma 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/59651-282-39





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