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Duloxetine

NDC 71610-957 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Marketing categoryANDA

Packages

71610-957-74 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-957-74)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-3062 — Duloxetine, 71335-3163 — Duloxetine, 71610-218 — DULOXETINE HYDROCHLORIDE, 71610-401 — Duloxetine Hydrochloride, 71610-402 — Duloxetine Hydrochloride, 71610-403 — Duloxetine, 71610-736 — DULOXETINE HYDROCHLORIDE, 71610-739 — DULOXETINE HYDROCHLORIDE, 71610-743 — DULOXETINE HYDROCHLORIDE, 71610-954 — 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, 72189-615 — Duloxetine D/R, 72189-634 — Duloxetine D/R, 72189-661 — Duloxetine D/R, 72789-338 — Duloxetine, +188 more

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