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"60687-734-01" National Drug Code (NDC)

Duloxetine 100 BLISTER PACK in 1 CARTON (60687-734-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-734-11)
(American Health Packaging)

NDC Code60687-734-01
Package Description100 BLISTER PACK in 1 CARTON (60687-734-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-734-11)
Product NDC60687-734
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20230403
Marketing Category NameANDA
Application NumberANDA090778
ManufacturerAmerican Health Packaging
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
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/60687-734-01





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