| NDC Code | 68788-7677-8 |
|---|
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7677-8) |
|---|
| Product NDC | 68788-7677 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Paroxetine |
|---|
| Non-Proprietary Name | Paroxetine Hydrochloride Hemihydrate |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200302 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203854 |
|---|
| Manufacturer | Preferred Pharmaceuticals, Inc. |
|---|
| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
|---|