Duloxetine
NDC 70954-864 · ANI Pharmaceuticals, Inc.
Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Marketing categoryANDA
Packages
70954-864-20 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70954-864-20)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
70518-1011 — Duloxetine, 70518-1054 — 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, 71205-005 — Duloxetine, 71205-358 — Duloxetine, 71205-445 — Duloxetine, 71205-525 — Duloxetine, 71205-602 — Duloxetine, 71335-0165 — DULOXETINE HYDROCHLORIDE, 71335-0392 — DULOXETINE HYDROCHLORIDE, 71335-0402 — Duloxetine, 71335-0509 — DULOXETINE HYDROCHLORIDE, 71335-1445 — Duloxetine, +188 more