Duloxetine 65841-0799
Product NDC
65841-0799- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 27, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA090739
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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(3)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-06)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-14)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-16)