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
- 0093-3547_8f789887-a198-4965-8582-e973d4da3994
- Product NDC
- 0093-3547
- Form
- CAPSULE
- Composition / generic term
- Atomoxetine
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170530
- Source listing expiry
- 20271231
Source-listed ingredients
- ATOMOXETINE HYDROCHLORIDE — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (0093-3547-56) · 0093-3547-56
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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