Duloxetine
- Product NDC
- 71610-957
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA090694
- Marketing category
- ANDA
- Substance
- DULOXETINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-957-74 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-957-74) | 2025-10-22 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Duloxetine | Aphena Pharma Solutions - Tennessee, LLC | 2025-10-22 | HUMAN PRESCRIPTION DRUG LABEL | 1 |