Duloxetine 31722-0169
Product NDC
31722-0169- Manufacturer
- Camber Pharmaceuticals, Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 30, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA204343
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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(6)
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-01)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-10)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-30)
7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-169-31)
105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-169-32)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-90)