Atomoxetine Hydrochloride
- Product NDC
- 50090-4237
- 11-digit product format
- 500904237
- Labeler code
- 50090
- Product ID
- 50090-4237_ebb8c17c-9b5f-4651-a8a3-b4be92b0b6aa
- 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
- 60 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4237 | ATOMOXETINE HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC | 20230208_11451684-b374-4e03-848c-a6da79b6979c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4237-0 | 50090423700 | 30 CAPSULE in 1 BOTTLE (50090-4237-0) | 30 capsule | 2019-03-29 | 0000-00-00 | No | No | Current |