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PAROXETINE
PAROXETINE - 49999-632-00 - (Paroxetine Hydrochloride)
Drug Information of PAROXETINE
| Product NDC: | 49999-632 |
| 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: | 49999-632 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077584 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111108 |
Package Information of PAROXETINE
| Package NDC: | 49999-632-00 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (49999-632-00) |
NDC Information of PAROXETINE
| NDC Code | 49999-632-00 |
| Proprietary Name | PAROXETINE |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (49999-632-00) |
| Product NDC | 49999-632 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Paroxetine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111108 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
