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
68002-105_56a6339d-4071-964f-e063-6394a90a786e
Product NDC
68002-105
Form
CAPSULE
Composition / generic term
Fluoxetine
Labeler
American Health Packaging
Marketing category
ANDA
Marketing start / end (source format)
20260714
Source listing expiry
20271231

Source-listed ingredients

  • FLUOXETINE HYDROCHLORIDE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 CARTON (68002-105-01) / 1 CAPSULE in 1 BLISTER PACK (68002-105-02) · 68002-105-01

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.

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