United States · FDA National Drug Code directory

PAROXETINE 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: 60505-1318_f641c7b3-f7d2-9446-e589-074ac368853a
Product NDC: 60505-1318
Form: TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term: paroxetine hydrochloride
Labeler: Apotex Corp
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20190809
Source listing expiry: 20261231

Source-listed ingredients

PAROXETINE HYDROCHLORIDE HEMIHYDRATE — 37.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1318-3) · 60505-1318-3

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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