Duloxetine 80425-0389
Product NDC
80425-0389- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 22, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA090694
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 60 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-1)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-2)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-3)