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Duloxetine

NDC 71610-736 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameDULOXETINE HYDROCHLORIDE
Dosage formCAPSULE, DELAYED RELEASE PELLETS
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

71610-736-42 — 1800 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-736-42)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2537 — Duloxetine, 71335-2567 — Duloxetine, 71335-2624 — Duloxetine, 71335-2625 — Duloxetine, 71335-3062 — Duloxetine, 71335-3163 — Duloxetine, 71610-218 — DULOXETINE HYDROCHLORIDE, 71610-401 — Duloxetine Hydrochloride, 71610-402 — Duloxetine Hydrochloride, 71610-403 — Duloxetine, 71610-739 — DULOXETINE HYDROCHLORIDE, 71610-743 — DULOXETINE HYDROCHLORIDE, 71610-954 — Duloxetine, 71610-957 — Duloxetine, 72162-1058 — Duloxetine, 72162-1597 — DULOXETINE HYDROCHLORIDE, 72162-1598 — DULOXETINE HYDROCHLORIDE, 72162-1599 — DULOXETINE HYDROCHLORIDE, 72162-1600 — DULOXETINE HYDROCHLORIDE, 72189-608 — Duloxetine D/R, +188 more

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