Fluoxetine
- Product NDC
- 55154-6890
- 11-digit product format
- 551546890
- Labeler code
- 55154
- Product ID
- 55154-6890_0c724fa9-f21e-4f5b-9db8-8c2ad0eb98cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076001
- Marketing category
- ANDA
- Marketing start
- 2007-02-16
- Marketing end
- 2019-03-31
- Substance
- FLUOXETINE HYDR
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reupt
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record