United States · FDA National Drug Code directory

Atomoxetine

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
64380-472_94ef88bd-e176-4c16-9340-ae0168422053
Product NDC
64380-472
Form
CAPSULE
Composition / generic term
Atomoxetine
Labeler
Strides Pharma Science Limited
Marketing category
ANDA
Marketing start / end (source format)
20250701
Source listing expiry
20271231

Source-listed ingredients

  • ATOMOXETINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE in 1 BOTTLE, PLASTIC (64380-472-01) · 64380-472-01
  • 500 CAPSULE in 1 BOTTLE, PLASTIC (64380-472-02) · 64380-472-02

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →