Fluoxetine
- Product NDC
- 63739-493
- 11-digit product format
- 637390493
- Labeler code
- 63739
- Product ID
- 63739-493_59de2889-c3d3-4ebf-8826-13f30a3fa439
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Capsules
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Packaging Services Business Unit of McKesson Corporation
- Application
- ANDA090223
- Marketing category
- ANDA
- Marketing start
- 2010-11-18
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 63739-493-40 | Fluoxetine | 100 in 1 BOTTLE | CAPSULE | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-493 | FLUOXETINE (FLUOXETINE CAPSULES) CAPSULE [MCKESSON PACKAGING SERVICES BUSINESS UNIT OF MCKESSON CORPORATION] | 1 | Legacy NDC, 1 package rows | 20101119_59de2889-c3d3-4ebf-8826-13f30a3fa439.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63739-493-40 | 63739049340 | 100 in 1 BOTTLE | Historical |