PAROXETINE
- Product NDC
- 60429-736
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paroxetine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075356
- Marketing category
- ANDA
- Substance
- PAROXETINE HYDROCHLORIDE ANHYDROUS
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 60429-736-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (60429-736-10) | 20190101 | | No | Historical |
| 60429-736-30 | 30 TABLET, FILM COATED in 1 BOTTLE (60429-736-30) | 20190101 | | No | Historical |
| 60429-736-90 | 90 TABLET, FILM COATED in 1 BOTTLE (60429-736-90) | 20190101 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| e63fe922-b35a-406c-8737-f3f5e6d5a30d | PAROXETINE TABLETS. These highlights do not include all the information needed to use PAROXETINE TABLETS safely and effectively. See full prescribing information for PAROXETINE TABLETS. PAROXETINE TABLETS, for oral use Initial U.S. Approval: 1992 | Golden State Medical Supply, Inc. | 2025-11-17 | HUMAN PRESCRIPTION DRUG LABEL | 16 |