FLUOXETINE
- Product NDC
- 68788-6794
- 11-digit product format
- 687886794
- Labeler code
- 68788
- Product ID
- 68788-6794_17929695-ed19-4937-a6c9-25d84746c493
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUOXETINE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA204597
- Marketing category
- ANDA
- Marketing start
- 2016-11-03
- 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