Duloxetine 68071-3766
Product NDC
68071-3766- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 16, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208706
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 30 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(1)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9)