"51991-747-10" National Drug Code (NDC)

Duloxetine 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-747-10
Package Description1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10)
Product NDC51991-747
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
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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