Duloxetine
NDC 68071-3775 · NuCare 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
68071-3775-9 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3775-9)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
67877-264 — Duloxetine, 67877-265 — Duloxetine, 68001-368 — DULOXETINE HYDROCHLORIDE, 68001-570 — Duloxetine, 68001-594 — Duloxetine, 68001-595 — Duloxetine, 68001-596 — Duloxetine, 68071-2711 — DULOXETINE HYDROCHLORIDE, 68071-3519 — Duloxetine, 68071-3766 — Duloxetine, 68071-3779 — Duloxetine, 68071-3979 — Duloxetine, 68180-294 — Duloxetine, 68180-295 — Duloxetine, 68180-296 — Duloxetine, 68180-297 — Duloxetine, 68788-4025 — Duloxetine, 68788-4026 — Duloxetine, 68788-4128 — Duloxetine, 68788-7672 — Duloxetine, +188 more