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"68084-675-21" National Drug Code (NDC)

Duloxetine 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-675-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-675-11)
(American Health Packaging)

NDC Code68084-675-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-675-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-675-11)
Product NDC68084-675
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131217
End Marketing Date20240430
Marketing Category NameANDA
Application NumberANDA090694
ManufacturerAmerican Health Packaging
Substance NameDULOXETINE HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-675-21





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