Sertraline Hydrochloride
- Product NDC
- 84386-098
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA077206
- Marketing category
- ANDA
- Substance
- SERTRALINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 84386-098-01 | 100 TABLET, FILM COATED in 1 BOTTLE (84386-098-01) | 2025-11-20 | | No | Historical |
| 84386-098-05 | 500 TABLET, FILM COATED in 1 BOTTLE (84386-098-05) | 2025-11-20 | | No | Historical |
| 84386-098-30 | 30 TABLET, FILM COATED in 1 BOTTLE (84386-098-30) | 2025-11-20 | | No | Historical |
| 84386-098-50 | 50 TABLET, FILM COATED in 1 BOTTLE (84386-098-50) | 2025-11-20 | | No | Historical |
| 84386-098-51 | 5000 TABLET, FILM COATED in 1 BOTTLE (84386-098-51) | 2025-11-20 | | No | Historical |
| 84386-098-60 | 60 TABLET, FILM COATED in 1 BOTTLE (84386-098-60) | 2025-11-20 | | No | Historical |
| 84386-098-90 | 90 TABLET, FILM COATED in 1 BOTTLE (84386-098-90) | 2025-11-20 | | No | Historical |
| 84386-098-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (84386-098-99) | 2025-11-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sertraline Hydrochloride | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED | 2025-11-24 | Human Prescription Drug Label | 1 |