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
- 69117-0024_472863af-ee04-24a6-e063-6394a90a9e20
- Product NDC
- 69117-0024
- Form
- TABLET, FILM COATED
- Composition / generic term
- Paroxetine
- Labeler
- Yiling Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211102
- Source listing expiry
- 20261231
Source-listed ingredients
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0024-1) · 69117-0024-1
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0024-2) · 69117-0024-2
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0024-3) · 69117-0024-3
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0024-4) · 69117-0024-4
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0024-5) · 69117-0024-5
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →