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
- 71335-1482_2ae53bb0-bc41-469a-8e7d-fa0801257e70
- Product NDC
- 71335-1482
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150316
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71335-1482-1) · 71335-1482-1
- 60 CAPSULE in 1 BOTTLE (71335-1482-2) · 71335-1482-2
- 100 CAPSULE in 1 BOTTLE (71335-1482-3) · 71335-1482-3
- 90 CAPSULE in 1 BOTTLE (71335-1482-4) · 71335-1482-4
- 28 CAPSULE in 1 BOTTLE (71335-1482-5) · 71335-1482-5
- 180 CAPSULE in 1 BOTTLE (71335-1482-6) · 71335-1482-6
- 120 CAPSULE in 1 BOTTLE (71335-1482-7) · 71335-1482-7
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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