Atomoxetine

NDC 0093-3542 · Teva Pharmaceuticals USA, Inc.

Generic nameAtomoxetine

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ATOMOXETINE HYDROCHLORIDE

Strength10 mg/1

Pharmacologic classNorepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]

Marketing categoryANDA

Packages

0093-3542-56 — 30 CAPSULE in 1 BOTTLE (0093-3542-56)

FDA lists these products with the same active ingredient.

0002-3227 — Atomoxetine hydrochloride, 0002-3228 — Atomoxetine hydrochloride, 0002-3229 — Atomoxetine hydrochloride, 0002-3238 — Atomoxetine hydrochloride, 0002-3239 — Atomoxetine hydrochloride, 0002-3250 — Atomoxetine hydrochloride, 0002-3251 — Atomoxetine hydrochloride, 0093-3543 — Atomoxetine, 0093-3544 — Atomoxetine, 0093-3545 — Atomoxetine, 0093-3546 — Atomoxetine, 0093-3547 — Atomoxetine, 0093-3548 — Atomoxetine, 0904-6908 — Atomoxetine, 16714-755 — atomoxetine, 16714-756 — atomoxetine, 16714-757 — atomoxetine, 16714-758 — atomoxetine, 16714-759 — atomoxetine, 16714-760 — atomoxetine, +116 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.