Fluoxetine
- Product NDC
- 70518-1775
- 11-digit product format
- 705181775
- Labeler code
- 70518
- Product ID
- 70518-1775_7eaab836-71d4-b6dd-e053-2991aa0a354e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076006
- Marketing category
- ANDA
- Marketing start
- 2019-01-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record