Fluoxetine
- Product NDC
- 50090-0744
- 11-digit product format
- 500900744
- Labeler code
- 50090
- Product ID
- 50090-0744_95e74c53-453b-4a8d-a624-af8a93c9e842
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076001
- Marketing category
- ANDA
- Marketing start
- 2002-01-29
- Marketing end
- 0000-00-00
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin 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 |
|---|
| 50090-0744 | FLUOXETINE CAPSULE [A-S MEDICATION SOLUTIONS] | 22 | Legacy NDC | 20230211_5670d52d-4447-453c-8546-db7f3eb57e1f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0744-0 | 50090074400 | 30 CAPSULE in 1 BOTTLE (50090-0744-0) | 30 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0744-1 | 50090074401 | 60 CAPSULE in 1 BOTTLE (50090-0744-1) | 60 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0744-3 | 50090074403 | 90 CAPSULE in 1 BOTTLE (50090-0744-3) | 90 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |