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Atomoxetine

NDC 55111-563 · Dr. Reddy's Laboratories Limited

Generic nameAtomoxetine
Dosage formCAPSULE
RouteORAL
Active ingredient(s)ATOMOXETINE HYDROCHLORIDE
Strength80 mg/1
Pharmacologic classNorepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
Marketing categoryANDA

Packages

55111-563-05 — 500 CAPSULE in 1 BOTTLE (55111-563-05)

55111-563-30 — 30 CAPSULE in 1 BOTTLE (55111-563-30)

55111-563-78 — 100 BLISTER PACK in 1 CARTON (55111-563-78) / 10 CAPSULE in 1 BLISTER PACK (55111-563-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 55111-522 — Atomoxetine, 55111-528 — Atomoxetine, 55111-564 — Atomoxetine, 60505-2830 — atomoxetine hydrochloride, 60505-2831 — atomoxetine hydrochloride, 60505-2832 — atomoxetine hydrochloride, 60505-2833 — atomoxetine hydrochloride, 60505-2834 — atomoxetine hydrochloride, 60505-2835 — atomoxetine hydrochloride, 60505-2836 — atomoxetine hydrochloride, 60687-326 — Atomoxetine, 60687-567 — 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.