Duloxetine 42708-0196
Product NDC
42708-0196- Manufacturer
- Qpharma, Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 11, 2013
- Listing Expires
- December 31, 2027
- Application
- ANDA090694
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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(1)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-196-30)