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Duloxetine

NDC 50090-6281 · 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

50090-6281-0 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6281-0)

50090-6281-1 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6281-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

47335-383 — Duloxetine, 47335-616 — Duloxetine, 47335-617 — Duloxetine, 47335-618 — Duloxetine, 47335-619 — Duloxetine, 49252-007 — duloxetine, 49252-008 — duloxetine, 49252-009 — duloxetine, 50090-3205 — DULOXETINE HYDROCHLORIDE, 50090-5940 — Duloxetine, 50090-6406 — Duloxetine, 50090-6775 — Duloxetine, 50090-6889 — DULOXETINE HYDROCHLORIDE, 50090-6893 — Duloxetine, 50090-6899 — Duloxetine, 50090-6900 — Duloxetine, 50090-7784 — Duloxetine, 50090-7812 — Duloxetine, 50090-7897 — Duloxetine, 50771-201 — DULOXETINE HYDROCHLORIDE, +188 more

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