PAROXETINE
- Product NDC
- 71610-992
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paroxetine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA075356
- Marketing category
- ANDA
- Substance
- PAROXETINE HYDROCHLORIDE ANHYDROUS
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-992-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-992-30) | 2026-03-17 | | No | Historical |
| 71610-992-45 | 45 TABLET, FILM COATED in 1 BOTTLE (71610-992-45) | 2026-03-17 | | No | Historical |
| 71610-992-53 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-992-53) | 2026-03-17 | | No | Historical |
| 71610-992-60 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-992-60) | 2026-03-17 | | No | Historical |