Atomoxetine
- Product NDC
- 72162-2543
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atomoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079021
- Marketing category
- ANDA
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2543-3 | 30 CAPSULE in 1 BOTTLE (72162-2543-3) | 2025-10-16 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Atomoxetine | Bryant Ranch Prepack | 2025-10-17 | HUMAN PRESCRIPTION DRUG LABEL | 101 |