Duloxetine Hydrochloride 46708-0279
Generic: Duloxetine
Product NDC
46708-0279- Manufacturer
- Alembic Pharmaceuticals Limited
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 9, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA202949
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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(3)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-30)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-90)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-91)