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Atomoxetine Hydrochloride

NDC 51407-102 · Golden State Medical Supply, Inc.

Generic nameatomoxetine hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)ATOMOXETINE HYDROCHLORIDE
Strength25 mg/1
Pharmacologic classNorepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

51407-102-30 — 30 CAPSULE in 1 BOTTLE (51407-102-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 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, 55111-522 — Atomoxetine, 55111-528 — Atomoxetine, 55111-563 — 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.