Duloxetine 47335-0381-86
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 11, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA090745
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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]
Selected Package
47335-0381-86Selected60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-86)
Other packages for this product(5)
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-08)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-18)
100 BLISTER PACK in 1 CARTON (47335-381-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-83)
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-88)