Duloxetine 71335-3062
Product NDC
71335-3062- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 16, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA208706
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 20 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(4)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-1)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-2)
28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-3)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-4)