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Atomoxetine

NDC 50090-6513 · A-S Medication Solutions

Generic nameAtomoxetine
Dosage formCAPSULE
RouteORAL
Active ingredient(s)ATOMOXETINE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classNorepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

50090-6513-0 — 30 CAPSULE in 1 BOTTLE (50090-6513-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42291-070 — Atomoxetine, 50090-4236 — atomoxetine hydrochloride, 50090-6127 — Atomoxetine, 50090-6143 — Atomoxetine, 50090-6144 — Atomoxetine, 50090-6254 — Atomoxetine, 50090-6289 — Atomoxetine, 50090-6444 — Atomoxetine, 50090-6511 — Atomoxetine, 50090-6512 — Atomoxetine, 50090-6703 — Atomoxetine, 50090-7342 — atomoxetine, 50090-7397 — atomoxetine, 50090-7462 — atomoxetine, 50090-7463 — atomoxetine, 50268-057 — atomoxetine hydrochloride, 50268-058 — atomoxetine hydrochloride, 50268-059 — atomoxetine hydrochloride, 51407-100 — atomoxetine hydrochloride, 51407-101 — atomoxetine hydrochloride, +116 more

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