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
- 83209-192_1fd02569-04f0-e34e-e063-6394a90a227b
- Product NDC
- 83209-192
- Form
- CAPSULE
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- Boswell Pharmacy Services LLC d/b/a BPS Wholesale
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240816
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CAPSULE in 1 BLISTER PACK (83209-192-10) · 83209-192-10
- 15 CAPSULE in 1 BLISTER PACK (83209-192-15) · 83209-192-15
- 30 CAPSULE in 1 BLISTER PACK (83209-192-30) · 83209-192-30
- 60 CAPSULE in 1 BLISTER PACK (83209-192-60) · 83209-192-60
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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