Fluoxetine
- Product NDC
- 51407-196
- 11-digit product format
- 514070196
- Labeler code
- 51407
- Product ID
- 51407-196_d3b194d1-3b3c-2714-e053-2995a90a9dac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUOXETINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA211282
- Marketing category
- ANDA
- Marketing start
- 2019-01-10
- Marketing end
- 0000-00-00
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-196-30 | 51407019630 | 30 TABLET in 1 BOTTLE (51407-196-30) | 30 tablet | 2019-02-25 | 0000-00-00 | No | No | Current |