Atomoxetine 68462-0265
Product NDC
68462-0265- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 30, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA079019
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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)
2000 CAPSULE in 1 BOTTLE (68462-265-23)
30 CAPSULE in 1 BOTTLE (68462-265-30)