Duloxetine 43547-0379
Product NDC
43547-0379- Manufacturer
- Solco Healthcare Us, Llc
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 20, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA206653
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 20 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(4)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-03)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-06)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-09)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-11)