"47335-820-18" National Drug Code (NDC)

Atomoxetine Hydrochloride 1000 CAPSULE in 1 BOTTLE (47335-820-18)
(Sun Pharma Global FZE)

NDC Code47335-820-18
Package Description1000 CAPSULE in 1 BOTTLE (47335-820-18)
Product NDC47335-820
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtomoxetine Hydrochloride
Non-Proprietary NameAtomoxetine Hydrochloride
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20101005
Marketing Category NameANDA
Application NumberANDA079020
ManufacturerSun Pharma Global FZE
Substance NameATOMOXETINE HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]

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