Duloxetine Delayed-Release 68788-8362
Generic: Duloxetine Hydrochloride
Product NDC
68788-8362- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA203088
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 40 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-0)
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-9)