Atomoxetine
- Product NDC
- 65862-240
- 11-digit product format
- 658620240
- Labeler code
- 65862
- Product ID
- 65862-240_48d5f73a-bdcc-466a-aa17-53c0a38c3b3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atomoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA079016
- Marketing category
- ANDA
- Marketing start
- 2017-05-30
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Norepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 57WVB6I2W0 | ATOMOXETINE HYDROCHLORIDE | 82248-59-7 | ATOMOXETINE HYDROCHLORIDE |
| ASW034S0B8 | ATOMOXETINE | 83015-26-3 | Atomoxetine |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 65862-240-22 | 65862024022 | 2000 CAPSULE in 1 BOTTLE (65862-240-22) | 2000 capsule | 2017-05-30 | No | No | Historical |
| 65862-240-30 | 65862024030 | 30 CAPSULE in 1 BOTTLE (65862-240-30) | 30 capsule | 2017-05-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Atomoxetine | Aurobindo Pharma Limited | 2025-12-12 | Human Prescription Drug Label | 16 |