"55700-505-30" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (55700-505-30)
(Lake Erie Medical DBA Quality Care Products LLC)

NDC Code55700-505-30
Package Description30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (55700-505-30)
Product NDC55700-505
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
ManufacturerLake Erie Medical DBA Quality Care Products LLC
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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