United States · FDA National Drug Code directory
Paroxetine
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
- 76420-717_2e000f86-0592-a362-e063-6394a90a169d
- Product NDC
- 76420-717
- Form
- TABLET, FILM COATED
- Composition / generic term
- Paroxetine
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070413
- Source listing expiry
- 20261231
Source-listed ingredients
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (76420-717-01) · 76420-717-01
- 500 TABLET, FILM COATED in 1 BOTTLE (76420-717-05) · 76420-717-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (76420-717-10) · 76420-717-10
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-717-30) · 76420-717-30
- 60 TABLET, FILM COATED in 1 BOTTLE (76420-717-60) · 76420-717-60
- 90 TABLET, FILM COATED in 1 BOTTLE (76420-717-90) · 76420-717-90
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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