Fluoxetine
- Product NDC
- 63629-6790
- 11-digit product format
- 636296790
- Labeler code
- 63629
- Product ID
- 63629-6790_c4e82dfc-10f6-4471-86e2-21da79ca97ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluoxetine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075755
- Marketing category
- ANDA
- Marketing start
- 2013-12-23
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6790-1 | 63629679001 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6790-1) | 2016-03-08 | 0000-00-00 | No | No | Current |
| 63629-6790-2 | 63629679002 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6790-2) | 2016-03-08 | 0000-00-00 | No | No | Current |