Duloxetine 51655-0237
Product NDC
51655-0237- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 23, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA208706
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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)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-25)