Duloxetine 67877-0263
Product NDC
67877-0263- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA203197
Need to source Duloxetine? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
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(5)
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-01)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-10)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-30)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-60)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-90)