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Paroxetine
Paroxetine - 13107-155-05 - (Paroxetine)
Drug Information of Paroxetine
| Product NDC: | 13107-155 |
| Proprietary Name: | Paroxetine |
| Non Proprietary Name: | Paroxetine |
| Active Ingredient(s): | 20 mg/1 & nbsp; Paroxetine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Paroxetine
| Product NDC: | 13107-155 |
| Labeler Name: | Aurolife Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078406 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091203 |
Package Information of Paroxetine
| Package NDC: | 13107-155-05 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (13107-155-05) |
NDC Information of Paroxetine
| NDC Code | 13107-155-05 |
| Proprietary Name | Paroxetine |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (13107-155-05) |
| Product NDC | 13107-155 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Paroxetine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091203 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurolife Pharma LLC |
| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
