Sertraline
- Product NDC
- 50090-7295
- 11-digit product format
- 500907295
- Labeler code
- 50090
- Product ID
- 50090-7295_c2e94e89-6016-4a0f-be9a-6eee53257a72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077670
- Marketing category
- ANDA
- Marketing start
- 2007-02-06
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| UTI8907Y6X | SERTRALINE HYDROCHLORIDE | 79559-97-0 | SERTRALINE HYDROCHLORIDE |
| QUC7NX6WMB | SERTRALINE | 79617-96-2 | Sertraline |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7295-0 | 50090729500 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7295-0) | 2024-10-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sertraline | A-S Medication Solutions | 2024-10-16 | HUMAN PRESCRIPTION DRUG LABEL | 9 |