Duloxetine
- Product NDC
- 71610-954
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA208706
- Marketing category
- ANDA
- Substance
- DULOXETINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-954-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-30) | 2025-10-14 | | No | Historical |
| 71610-954-53 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-53) | 2025-10-14 | | No | Historical |
| 71610-954-60 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-60) | 2025-10-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Duloxetine | Aphena Pharma Solutions - Tennessee, LLC | 2025-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 1 |