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
- 72162-1495_5d2b1d8a-f878-44f2-98b1-c95ccc8990e7
- Product NDC
- 72162-1495
- Form
- TABLET, COATED
- Composition / generic term
- fluoxetine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160822
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOXETINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1495-1) · 72162-1495-1
- 30 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1495-3) · 72162-1495-3
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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