atomoxetine
- Product NDC
- 70518-2474
- 11-digit product format
- 705182474
- Labeler code
- 70518
- Product ID
- 70518-2474_c9605376-7e12-58ff-e053-2a95a90a3c51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atomoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA079019
- Marketing category
- ANDA
- Marketing start
- 2019-12-09
- Marketing end
- 0000-00-00
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2474-0 | 70518247400 | 30 POUCH in 1 BOX (70518-2474-0) > 1 CAPSULE in 1 POUCH (70518-2474-1) | 30 pouch | 2019-12-09 | 0000-00-00 | No | No | Current |