United States · FDA National Drug Code directory
Atomoxetine Hydrochloride
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
- 60505-2832_c668f0bc-71d1-fa44-32db-35fa6fc027a2
- Product NDC
- 60505-2832
- Form
- CAPSULE
- Composition / generic term
- atomoxetine hydrochloride
- Labeler
- Apotex Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180521
- Source listing expiry
- 20271231
Source-listed ingredients
- ATOMOXETINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (60505-2832-3) · 60505-2832-3
Source and coverage
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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.
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