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Duloxetine

NDC 76420-633 · Asclemed USA, Inc.

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

76420-633-00 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-00)

76420-633-01 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-01)

76420-633-05 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-05)

76420-633-20 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-20)

76420-633-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-30)

76420-633-60 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-60)

76420-633-90 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 76420-236 — Duloxetine, 76420-623 — 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, 80425-0389 — Duloxetine, 80425-0441 — 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.