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PAROXETINE HYDROCHLORIDE
PAROXETINE HYDROCHLORIDE - 60505-3675-3 - (paroxetine hydrochloride)
Drug Information of PAROXETINE HYDROCHLORIDE
| Product NDC: | 60505-3675 |
| Proprietary Name: | PAROXETINE HYDROCHLORIDE |
| Non Proprietary Name: | paroxetine hydrochloride |
| Active Ingredient(s): | 37.5 mg/1 & nbsp; paroxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PAROXETINE HYDROCHLORIDE
| Product NDC: | 60505-3675 |
| Labeler Name: | Apotex Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020936 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100913 |
Package Information of PAROXETINE HYDROCHLORIDE
| Package NDC: | 60505-3675-3 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3675-3) |
NDC Information of PAROXETINE HYDROCHLORIDE
| NDC Code | 60505-3675-3 |
| Proprietary Name | PAROXETINE HYDROCHLORIDE |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3675-3) |
| Product NDC | 60505-3675 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | paroxetine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100913 |
| Marketing Category Name | NDA |
| Labeler Name | Apotex Corp |
| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
| Strength Number | 37.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
