Duloxetine

NDC 50090-7784 · A-S Medication Solutions

Generic nameDuloxetine

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)DULOXETINE HYDROCHLORIDE

Strength30 mg/1

Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Marketing categoryANDA

Packages

50090-7784-0 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7784-0)

FDA lists these products with the same active ingredient.

49252-009 — duloxetine, 50090-3205 — DULOXETINE HYDROCHLORIDE, 50090-5940 — Duloxetine, 50090-6281 — Duloxetine, 50090-6406 — Duloxetine, 50090-6775 — Duloxetine, 50090-6889 — DULOXETINE HYDROCHLORIDE, 50090-6893 — Duloxetine, 50090-6899 — Duloxetine, 50090-6900 — 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, 51407-809 — Duloxetine, 51407-810 — Duloxetine, 51407-817 — DULOXETINE HYDROCHLORIDE, +188 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.