Duloxetine 76420-0636
Product NDC
76420-0636- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 25, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA208706
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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(4)
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-01)
20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-20)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-30)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-90)