Fluoxetine
- Product NDC
- 63629-6770
- 11-digit product format
- 636296770
- Labeler code
- 63629
- Product ID
- 63629-6770_dcd691e6-85cf-46f7-ac81-b7ae709d6fd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076001
- Marketing category
- ANDA
- Marketing start
- 2002-01-29
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6770-1 | 63629677001 | 30 CAPSULE in 1 BOTTLE (63629-6770-1) | 30 capsule | 2015-09-15 | 0000-00-00 | No | No | Current |
| 63629-6770-2 | 63629677002 | 60 CAPSULE in 1 BOTTLE (63629-6770-2) | 60 capsule | 2015-09-15 | 0000-00-00 | No | No | Current |
| 63629-6770-3 | 63629677003 | 90 CAPSULE in 1 BOTTLE (63629-6770-3) | 90 capsule | 2015-09-15 | 0000-00-00 | No | No | Current |