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
- 82619-120_587648dc-7a8b-43a9-e063-6294a90a620b
- Product NDC
- 82619-120
- Form
- CAPSULE
- Composition / generic term
- atomoxetine
- Labeler
- Creekwood Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260706
- 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 (82619-120-01) · 82619-120-01
- 1000 CAPSULE in 1 BOTTLE (82619-120-02) · 82619-120-02
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 →