Duloxetine 71205-0602
Product NDC
71205-0602- Manufacturer
- Proficient Rx Lp
- 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(3)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-30)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-60)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)