Duloxetine
NDC 50090-6893 · A-S Medication Solutions
Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Marketing categoryANDA
Packages
50090-6893-0 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6893-0)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
47335-619 — Duloxetine, 49252-007 — duloxetine, 49252-008 — duloxetine, 49252-009 — duloxetine, 50090-3205 — DULOXETINE HYDROCHLORIDE, 50090-5940 — Duloxetine, 50090-6281 — Duloxetine, 50090-6406 — Duloxetine, 50090-6775 — Duloxetine, 50090-6889 — DULOXETINE HYDROCHLORIDE, 50090-6899 — Duloxetine, 50090-6900 — Duloxetine, 50090-7784 — Duloxetine, 50090-7812 — Duloxetine, 50090-7897 — Duloxetine, 50771-201 — DULOXETINE HYDROCHLORIDE, 50771-202 — DULOXETINE HYDROCHLORIDE, 50771-203 — DULOXETINE HYDROCHLORIDE, 51407-807 — Duloxetine, 51407-808 — Duloxetine, +188 more