| NDC Code | 60505-3674-3 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3674-3) |
|---|
| Product NDC | 60505-3674 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Paroxetine Hydrochloride |
|---|
| Non-Proprietary Name | Paroxetine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100913 |
|---|
| End Marketing Date | 20230131 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020936 |
|---|
| Manufacturer | Apotex Corp |
|---|
| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
|---|