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
- 60429-737_52d4a27a-f543-6e04-e063-6394a90afc87
- Product NDC
- 60429-737
- Form
- TABLET, FILM COATED
- Composition / generic term
- paroxetine hydrochloride
- Labeler
- Golden State Medical Supply, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20030730
- Source listing expiry
- 20271231
Source-listed ingredients
- PAROXETINE HYDROCHLORIDE ANHYDROUS — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (60429-737-10) · 60429-737-10
- 30 TABLET, FILM COATED in 1 BOTTLE (60429-737-30) · 60429-737-30
- 90 TABLET, FILM COATED in 1 BOTTLE (60429-737-90) · 60429-737-90
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 →