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
- 71335-1548_c1d88c7e-4490-4618-9d78-93be301e14c6
- Product NDC
- 71335-1548
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150316
- 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 (71335-1548-1) · 71335-1548-1
- 90 CAPSULE in 1 BOTTLE (71335-1548-2) · 71335-1548-2
- 60 CAPSULE in 1 BOTTLE (71335-1548-3) · 71335-1548-3
- 120 CAPSULE in 1 BOTTLE (71335-1548-4) · 71335-1548-4
- 28 CAPSULE in 1 BOTTLE (71335-1548-5) · 71335-1548-5
- 15 CAPSULE in 1 BOTTLE (71335-1548-6) · 71335-1548-6
- 100 CAPSULE in 1 BOTTLE (71335-1548-7) · 71335-1548-7
- 180 CAPSULE in 1 BOTTLE (71335-1548-8) · 71335-1548-8
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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