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Duloxetine

NDC 68180-296 · Lupin 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

68180-296-03 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-03)

68180-296-06 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-06)

68180-296-09 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-595 — Duloxetine, 68001-596 — Duloxetine, 68071-2711 — DULOXETINE HYDROCHLORIDE, 68071-3519 — Duloxetine, 68071-3766 — Duloxetine, 68071-3775 — Duloxetine, 68071-3779 — Duloxetine, 68071-3979 — Duloxetine, 68180-294 — Duloxetine, 68180-295 — Duloxetine, 68180-297 — Duloxetine, 68788-4025 — Duloxetine, 68788-4026 — Duloxetine, 68788-4128 — Duloxetine, 68788-7672 — Duloxetine, 68788-7897 — DULOXETINE HYDROCHLORIDE, 68788-7935 — Duloxetine, 68788-8362 — DULOXETINE HYDROCHLORIDE, 68788-8608 — Duloxetine, 68788-8623 — 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.