Paroxetine
- Product NDC
- 55154-5087
- 11-digit product format
- 551545087
- Labeler code
- 55154
- Product ID
- 55154-5087_639297f7-99af-416e-89e3-2abfcdb55abe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paroxetine hydrochloride hemihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078902
- Marketing category
- ANDA
- Marketing start
- 2011-01-14
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X2ELS050D8 | PAROXETINE HYDROCHLORIDE HEMIHYDRATE | 110429-35-1 | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |