Fluoxetine
- Product NDC
- 45865-368
- 11-digit product format
- 458650368
- Labeler code
- 45865
- Product ID
- 45865-368_715e646a-a543-d53c-e053-2a95a90a46dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA078619
- Marketing category
- ANDA
- Marketing start
- 2008-01-31
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45865-368-30 | Fluoxetine | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
| 45865-368-51 | Fluoxetine | 120 in 1 BOTTLE | CAPSULE | 120 | | 1 |
| 45865-368-60 | Fluoxetine | 60 in 1 BOTTLE | CAPSULE | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-368 | FLUOXETINE (FLUOXETINE HYDROCHLORIDE) CAPSULE [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 3 package rows | 20180720_715e9083-f5c4-500f-e053-2a95a90a1436.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-368-30 | 45865036830 | 30 in 1 BOTTLE | Historical |
| 45865-368-51 | 45865036851 | 120 in 1 BOTTLE | Historical |
| 45865-368-60 | 45865036860 | 60 in 1 BOTTLE | Historical |