www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"60687-723-21" National Drug Code (NDC)

Duloxetine 30 BLISTER PACK in 1 CARTON (60687-723-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-723-11)
(American Health Packaging)

NDC Code60687-723-21
Package Description30 BLISTER PACK in 1 CARTON (60687-723-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-723-11)
Product NDC60687-723
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20230425
Marketing Category NameANDA
Application NumberANDA090778
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/60687-723-21





Copyright © 2007-2024 www.ndcvalidator.com