United States · FDA National Drug Code directory
FLUOXETINE
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
- 68788-8618_ec67d3fd-5f16-4fc1-b174-90ede65171a0
- Product NDC
- 68788-8618
- Form
- CAPSULE
- Composition / generic term
- FLUOXETINE
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240328
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (68788-8618-1) · 68788-8618-1
- 30 CAPSULE in 1 BOTTLE (68788-8618-3) · 68788-8618-3
- 90 CAPSULE in 1 BOTTLE (68788-8618-6) · 68788-8618-6
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 →