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Duloxetine

NDC 76420-236 · Asclemed USA, Inc.

Generic nameDuloxetine
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

76420-236-30 — 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-30)

76420-236-60 — 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-60)

76420-236-90 — 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 76420-623 — Duloxetine, 76420-633 — Duloxetine, 76420-634 — Duloxetine, 76420-636 — Duloxetine, 80425-0012 — Duloxetine HCL, 80425-0014 — Duloxetine HCL, 80425-0086 — Duloxetine HCL, 80425-0119 — Duloxetine, 80425-0146 — Duloxetine HCL, 80425-0311 — 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.