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
- 71335-0924_ffe74518-5a6e-4a92-ae3f-41fb7af9b642
- Product NDC
- 71335-0924
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020129
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71335-0924-1) · 71335-0924-1
- 100 CAPSULE in 1 BOTTLE (71335-0924-2) · 71335-0924-2
- 60 CAPSULE in 1 BOTTLE (71335-0924-3) · 71335-0924-3
- 15 CAPSULE in 1 BOTTLE (71335-0924-4) · 71335-0924-4
- 56 CAPSULE in 1 BOTTLE (71335-0924-5) · 71335-0924-5
- 28 CAPSULE in 1 BOTTLE (71335-0924-6) · 71335-0924-6
- 90 CAPSULE in 1 BOTTLE (71335-0924-7) · 71335-0924-7
- 120 CAPSULE in 1 BOTTLE (71335-0924-8) · 71335-0924-8
- 45 CAPSULE in 1 BOTTLE (71335-0924-9) · 71335-0924-9
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 →