Atomoxetine 82619-0115
Product NDC
82619-0115- Manufacturer
- Creekwood Pharmaceuticals Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 6, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA218875
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Atomoxetine Hydrochloride | 10 mg/1 |
Drug Class
Norepinephrine Reuptake Inhibitor [EPC]Norepinephrine Uptake Inhibitors [MoA]
Packaging Options(2)
30 CAPSULE in 1 BOTTLE (82619-115-01)
500 CAPSULE in 1 BOTTLE (82619-115-02)