Fluoxetine Hydrochloride
- Product NDC
- 63629-6855
- 11-digit product format
- 636296855
- Labeler code
- 63629
- Product ID
- 63629-6855_b47b1d1d-42b3-43ec-a841-b4bf02343877
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075049
- Marketing category
- ANDA
- Marketing start
- 2001-08-02
- 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
- 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 |
|---|
| 63629-6855-1 | 63629685501 | 30 CAPSULE in 1 BOTTLE (63629-6855-1) | 30 capsule | 2015-11-18 | 0000-00-00 | No | No | Current |
| 63629-6855-2 | 63629685502 | 90 CAPSULE in 1 BOTTLE (63629-6855-2) | 90 capsule | 2015-11-18 | 0000-00-00 | No | No | Current |