Sertraline
- Product NDC
- 50090-7614
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076465
- Marketing category
- ANDA
- Substance
- SERTRALINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7614-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7614-0) | 2025-07-23 | | No | Historical |
| 50090-7614-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7614-1) | 2025-07-23 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sertraline | A-S Medication Solutions | 2026-03-02 | HUMAN PRESCRIPTION DRUG LABEL | 4 |