Sertraline HCL
- Product NDC
- 72189-551
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline HCL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077206
- Marketing category
- ANDA
- Substance
- SERTRALINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-551-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-551-30) | 2024-05-01 | | No | Historical |
| 72189-551-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-551-90) | 2024-05-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sertraline HCL | Direct_Rx | 2024-05-16 | HUMAN PRESCRIPTION DRUG LABEL | 2 |