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"47335-382-83" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-83)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-382-83
Package Description30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-83)
Product NDC47335-382
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
Strength30
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/47335-382-83





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