Duloxetine
- Product NDC
- 68071-3775
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA090694
- Marketing category
- ANDA
- Substance
- DULOXETINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3775-9 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3775-9) | 2025-01-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Duloxetine | NuCare Pharmaceuticals, Inc. | 2025-01-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |