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Paroxetine
Paroxetine - 0093-7115-98 - (Paroxetine Hydrochloride)
Drug Information of Paroxetine
| Product NDC: | 0093-7115 |
| Proprietary Name: | Paroxetine |
| Non Proprietary Name: | Paroxetine Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Paroxetine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Paroxetine
| Product NDC: | 0093-7115 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076618 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051003 |
Package Information of Paroxetine
| Package NDC: | 0093-7115-98 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (0093-7115-98) |
NDC Information of Paroxetine
| NDC Code | 0093-7115-98 |
| Proprietary Name | Paroxetine |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (0093-7115-98) |
| Product NDC | 0093-7115 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Paroxetine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20051003 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | PAROXETINE HYDROCHLORIDE ANHYDROUS |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
