Duloxetine Hydrochloride 73476-0747
Product NDC
73476-0747- Manufacturer
- Towa Pharmaceutical Europe, S.l.
- Dosage Form
- Capsule, Delayed Release Pellets
- Product Type
- Drug For Further Processing
- Marketing Start
- January 29, 2016
- Listing Expires
- December 31, 2026
Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 30 mg/1 |
Packaging Options(1)
100000 CAPSULE, DELAYED RELEASE PELLETS in 1 DRUM (73476-747-00)