Paroxetine
- Product NDC
- 55154-4753
- 11-digit product format
- 551544753
- Labeler code
- 55154
- Product ID
- 55154-4753_6a90e0df-7430-461f-8be4-b385eeacdfbd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paroxetine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077584
- Marketing category
- ANDA
- Marketing start
- 2011-05-19
- Marketing end
- 2020-10-31
- Substance
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record