"55700-435-30" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-435-30)
(Lake Erie Medical DBA Quality Care Products LLC)

NDC Code55700-435-30
Package Description30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-435-30)
Product NDC55700-435
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140820
Marketing Category NameANDA
Application NumberANDA202045
ManufacturerLake Erie Medical DBA Quality Care Products LLC
Substance NameDULOXETINE HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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