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"64725-0747-1" National Drug Code (NDC)

Duloxetine 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (64725-0747-1)
(TYA Pharmaceuticals)

NDC Code64725-0747-1
Package Description90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (64725-0747-1)
Product NDC64725-0747
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Proprietary Name SuffixDelayed-release
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20140611
Marketing Category NameANDA
Application NumberANDA203088
ManufacturerTYA Pharmaceuticals
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/64725-0747-1





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