Duloxetine 49252-0007
Product NDC
49252-0007- Manufacturer
- Inventia Healthcare Limited.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA202336
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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(5)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-10)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-11)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-12)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-18)
100 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (49252-007-57)