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"47335-383-61" National Drug Code (NDC)

Duloxetine 100 BLISTER PACK in 1 CARTON (47335-383-61) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-383-61
Package Description100 BLISTER PACK in 1 CARTON (47335-383-61) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC47335-383
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131211
Marketing Category NameANDA
Application NumberANDA090745
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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