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
- 25000-147_46219345-2dd8-4502-a0fc-1631e354dc98
- Product NDC
- 25000-147
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- MARKSANS PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220129
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (25000-147-03) · 25000-147-03
- 100 CAPSULE in 1 BOTTLE (25000-147-08) · 25000-147-08
- 1000 CAPSULE in 1 BOTTLE (25000-147-14) · 25000-147-14
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 →