Duloxetine 68001-0595
Product NDC
68001-0595- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 28, 2023
- 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(3)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-04)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-05)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-08)