Sertraline Hydrochloride
- Product NDC
- 70518-4590
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077670
- Marketing category
- ANDA
- Substance
- SERTRALINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70518-4590-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4590-0) | 2026-03-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sertraline Hydrochloride | REMEDYREPACK INC. | 2026-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |