Duloxetine 70247-0014
Product NDC
70247-0014- Manufacturer
- Qingdao Baheal Pharmaceutical Co., Ltd.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 5, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210599
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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(3)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-03)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-06)
500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-50)