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
- 71335-1145_b49e52e9-9e47-498f-9c7b-83790ecd742c
- Product NDC
- 71335-1145
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080131
- 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 (71335-1145-1) · 71335-1145-1
- 60 CAPSULE in 1 BOTTLE (71335-1145-2) · 71335-1145-2
- 100 CAPSULE in 1 BOTTLE (71335-1145-3) · 71335-1145-3
- 90 CAPSULE in 1 BOTTLE (71335-1145-4) · 71335-1145-4
- 28 CAPSULE in 1 BOTTLE (71335-1145-5) · 71335-1145-5
- 180 CAPSULE in 1 BOTTLE (71335-1145-6) · 71335-1145-6
- 120 CAPSULE in 1 BOTTLE (71335-1145-7) · 71335-1145-7
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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