Atomoxetine

NDC 31722-716 · Camber Pharmaceuticals, Inc.

Generic nameAtomoxetine

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ATOMOXETINE HYDROCHLORIDE

Strength25 mg/1

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

Marketing categoryANDA

Packages

31722-716-30 — 30 CAPSULE in 1 BOTTLE (31722-716-30)

FDA lists these products with the same active ingredient.

16714-755 — atomoxetine, 16714-756 — atomoxetine, 16714-757 — atomoxetine, 16714-758 — atomoxetine, 16714-759 — atomoxetine, 16714-760 — atomoxetine, 16714-761 — atomoxetine, 30698-456 — Atomoxetine hydrochloride, 31722-714 — Atomoxetine, 31722-715 — Atomoxetine, 31722-717 — Atomoxetine, 31722-718 — Atomoxetine, 31722-719 — Atomoxetine, 31722-720 — Atomoxetine, 42291-064 — Atomoxetine, 42291-065 — Atomoxetine, 42291-066 — Atomoxetine, 42291-067 — Atomoxetine, 42291-068 — Atomoxetine, 42291-069 — 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.