Atomoxetine

NDC 72603-436 · NorthStar RxLLC

Generic nameAtomoxetine

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ATOMOXETINE HYDROCHLORIDE

Strength18 mg/1

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

Marketing categoryANDA

Packages

72603-436-01 — 30 CAPSULE in 1 BOTTLE (72603-436-01)

FDA lists these products with the same active ingredient.

71335-3033 — Atomoxetine, 71335-9702 — Atomoxetine, 72162-2541 — Atomoxetine, 72162-2542 — Atomoxetine, 72162-2543 — Atomoxetine, 72162-2544 — Atomoxetine, 72162-2545 — Atomoxetine, 72162-2546 — Atomoxetine, 72162-2547 — Atomoxetine, 72603-435 — Atomoxetine, 72603-437 — Atomoxetine, 72603-438 — Atomoxetine, 72603-439 — Atomoxetine, 72603-440 — Atomoxetine, 72603-441 — Atomoxetine, 72888-456 — Atomoxetine hydrochloride, 82619-115 — atomoxetine, 82619-116 — atomoxetine, 82619-117 — atomoxetine, 82619-118 — atomoxetine, +116 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.