Duloxetine Hydrochloride 33342-0160
Product NDC
33342-0160- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 24, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA204815
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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)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-09)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-10)
10 BLISTER PACK in 1 CARTON (33342-160-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-44)