Duloxetine 71205-0525
Product NDC
71205-0525- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 17, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA090776
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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(3)
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30)
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60)
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90)