"64725-1100-1" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (64725-1100-1)
(TYA Pharmaceuticals)

NDC Code64725-1100-1
Package Description30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (64725-1100-1)
Product NDC64725-1100
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetin Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131211
Marketing Category NameANDA
Application NumberANDA090774
ManufacturerTYA Pharmaceuticals
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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