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
- 13668-473_f8d8c930-c8f9-4186-92fa-6f7a5dabe083
- Product NDC
- 13668-473
- Form
- TABLET
- Composition / generic term
- Fluoxetine
- Labeler
- Torrent Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161021
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (13668-473-01) · 13668-473-01
- 1000 TABLET in 1 BOTTLE (13668-473-10) · 13668-473-10
- 30 TABLET in 1 BOTTLE (13668-473-30) · 13668-473-30
- 100 TABLET in 1 CARTON (13668-473-74) · 13668-473-74
- 28 TABLET in 1 CARTON (13668-473-91) · 13668-473-91
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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