Atomoxetine Hydrochloride
- Product NDC
- 50090-4244
- 11-digit product format
- 500904244
- Labeler code
- 50090
- Product ID
- 50090-4244_052d3c03-1f11-4c43-81ac-27d44c90f61b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atomoxetine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078983
- Marketing category
- ANDA
- Marketing start
- 2018-05-21
- Marketing end
- 0000-00-00
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Active strength
- 100 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4244-0 | 50090424400 | 30 CAPSULE in 1 BOTTLE (50090-4244-0) | 30 capsule | 2019-03-29 | 0000-00-00 | No | No | Current |