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Duloxetine

NDC 87063-704 · ASCLEMED USA INC.

Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Marketing categoryANDA

Packages

87063-704-12 — 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-12)

87063-704-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-30)

87063-704-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-60)

87063-704-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

80425-0389 — Duloxetine, 80425-0441 — Duloxetine, 82009-029 — DULOXETINE HYDROCHLORIDE, 82009-030 — DULOXETINE HYDROCHLORIDE, 82009-031 — DULOXETINE HYDROCHLORIDE, 82009-032 — DULOXETINE HYDROCHLORIDE, 82009-170 — Duloxetine, 82009-171 — Duloxetine, 82009-172 — Duloxetine, 82009-173 — Duloxetine, 82804-024 — DULOXETINE HYDROCHLORIDE, 85534-0016 — Duloxetine, 85534-0017 — Duloxetine, 85534-0018 — Duloxetine, 85534-0050 — Duloxetine, 85534-0051 — Duloxetine, 85534-0052 — Duloxetine, 85534-0053 — Duloxetine, 87063-702 — Duloxetine, 87063-703 — 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.