Fluoxetine
- Product NDC
- 50090-2793
- 11-digit product format
- 500902793
- Labeler code
- 50090
- Product ID
- 50090-2793_e065137f-3354-4fb1-952f-6dedfd98d26d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078619
- Marketing category
- ANDA
- Marketing start
- 2008-01-31
- Marketing end
- 0000-00-00
- Substance
- FLUOXETINE HYDR
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reupt
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2793-0 | Fluoxetine | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 25 |
| 50090-2793-0 | Fluoxetine | 32 in 1 BOX, UNIT-DOSE | CAPSULE | 32 | | 25 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2793 | FLUOXETINE (FLUOXETINE HYDROCHLORIDE) CAPSULE [A-S MEDICATION SOLUTIONS] | 25 | Legacy NDC, 2 package rows | 20241010_42c4c341-8282-4961-8581-8a0430162559.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2793-0 | 50090279300 | 1 in 1 BLISTER PACK | Historical |