0615-8494Level 3
Duloxetine (Duloxetine)
**Product type:** Human Prescription Drug
**Active ingredient:** DULOXETINE HYDROCHLORIDE
**Strength:** 20 mg/1
**Dosage form:** Capsule, Delayed Release
**Route:** Oral
**Labeler:** NCS HealthCare of KY, LLC dba Vangard Labs
**Marketing category:** ANDA (ANDA090694)
**Pharmacologic class:** Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
GET
/api/v1/systems/ndc_fda/nodes/0615-8494Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.