United States · FDA National Drug Code directory
Fluoxetine hydrochloride
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
- 55111-284_42f4ab4e-3271-f7cc-8e57-e621d0d3e1d5
- Product NDC
- 55111-284
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- Fluoxetine Hydrochloride
- Labeler
- Dr.Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100324
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 90 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK · 55111-284-48
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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