Fluoxetine
- Product NDC
- 50090-3180
- 11-digit product format
- 500903180
- Labeler code
- 50090
- Product ID
- 50090-3180_b3afa680-0b29-43bf-adb9-bb1c7131f301
- 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
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3180 | FLUOXETINE CAPSULE [A-S MEDICATION SOLUTIONS] | 22 | Legacy NDC | 20230211_5670d52d-4447-453c-8546-db7f3eb57e1f.zip |