Duloxetine 70518-3287
Product NDC
70518-3287- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 9, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA208706
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 30 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(4)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-0)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-2)
50 POUCH in 1 BOX (70518-3287-3) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-3287-4)
50 POUCH in 1 BOX (70518-3287-5) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-3287-6)