Atomoxetine Hydrochloride

NDC 50268-059 · AvPAK

Generic nameatomoxetine hydrochloride

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ATOMOXETINE HYDROCHLORIDE

Strength60 mg/1

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

Marketing categoryANDA

Packages

50268-059-13 — 30 BLISTER PACK in 1 BOX (50268-059-13) / 1 CAPSULE in 1 BLISTER PACK (50268-059-11)

FDA lists these products with the same active ingredient.

50090-6511 — Atomoxetine, 50090-6512 — Atomoxetine, 50090-6513 — Atomoxetine, 50090-6703 — Atomoxetine, 50090-7342 — atomoxetine, 50090-7397 — atomoxetine, 50090-7462 — atomoxetine, 50090-7463 — atomoxetine, 50268-057 — atomoxetine hydrochloride, 50268-058 — atomoxetine hydrochloride, 51407-100 — atomoxetine hydrochloride, 51407-101 — atomoxetine hydrochloride, 51407-102 — atomoxetine hydrochloride, 51407-103 — atomoxetine hydrochloride, 51407-104 — atomoxetine hydrochloride, 51407-105 — atomoxetine hydrochloride, 51407-106 — atomoxetine hydrochloride, 55111-519 — Atomoxetine, 55111-520 — Atomoxetine, 55111-521 — 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.