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Duloxetine

NDC 70518-1054 · REMEDYREPACK INC.

Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
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

70518-1054-0 — 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-0)

70518-1054-6 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-6)

70518-1054-7 — 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-7)

70518-1054-9 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-7935 — Duloxetine, 68788-8362 — DULOXETINE HYDROCHLORIDE, 68788-8608 — Duloxetine, 68788-8623 — Duloxetine, 68788-8782 — Duloxetine, 70247-012 — Duloxetine, 70247-013 — Duloxetine, 70247-014 — Duloxetine, 70518-0122 — DULOXETINE HYDROCHLORIDE, 70518-1011 — Duloxetine, 70518-1139 — Duloxetine, 70518-1244 — Duloxetine, 70518-1765 — Duloxetine, 70518-2630 — Duloxetine, 70518-3287 — Duloxetine, 70518-4440 — Duloxetine, 70954-860 — Duloxetine, 70954-861 — Duloxetine, 70954-864 — Duloxetine, 71205-005 — 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.