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: 49884-335_caca8641-502e-40dd-a219-2eb49188413f
Product NDC: 49884-335
Form: TABLET, COATED
Composition / generic term: fluoxetine hydrochloride
Labeler: Par Health USA, LLC
Marketing category: ANDA
Marketing start / end (source format): 20160822
Source listing expiry: 20271231

Source-listed ingredients

FLUOXETINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-01) · 49884-335-01
30 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-11) · 49884-335-11

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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