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
- 70518-0417_5519b4bb-ba0c-cd58-e063-6294a90ab317
- Product NDC
- 70518-0417
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170410
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BLISTER PACK (70518-0417-1) · 70518-0417-1
- 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-2) · 70518-0417-2
- 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-3) · 70518-0417-3
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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