Duloxetine Hydrochloride 00110-3235
Product NDC
00110-3235- Manufacturer
- Lilly Del Caribe, Inc.
- Dosage Form
- Capsule, Delayed Release
- Product Type
- Drug For Further Processing
- Marketing Start
- August 24, 2004
- Listing Expires
- December 31, 2026
Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 20 mg/1 |
Packaging Options(1)
300000 CAPSULE, DELAYED RELEASE in 1 DRUM (0110-3235-05)