Duloxetine 00228-2892
Product NDC
00228-2892- Manufacturer
- Actavis Pharma, Inc.
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 17, 2013
- Listing Expires
- December 31, 2027
- Application
- ANDA090776
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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(2)
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2892-03)
1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2892-96)