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
- 68382-218_8e543a65-7611-4362-94ba-0b3f929c776c
- Product NDC
- 68382-218
- Form
- CAPSULE
- Composition / generic term
- atomoxetine
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170612
- Source listing expiry
- 20261231
Source-listed ingredients
- ATOMOXETINE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2000 CAPSULE in 1 BOTTLE (68382-218-02) · 68382-218-02
- 30 CAPSULE in 1 BOTTLE (68382-218-06) · 68382-218-06
- 1000 CAPSULE in 1 BOTTLE (68382-218-10) · 68382-218-10
- 60 CAPSULE in 1 BOTTLE (68382-218-14) · 68382-218-14
- 90 CAPSULE in 1 BOTTLE (68382-218-16) · 68382-218-16
- 10 BLISTER PACK in 1 CARTON (68382-218-77) / 10 CAPSULE in 1 BLISTER PACK (68382-218-30) · 68382-218-77
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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