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Zoloft
Zoloft - 55154-2709-0 - (sertraline hydrochloride)
Drug Information of Zoloft
| Product NDC: | 55154-2709 |
| Proprietary Name: | Zoloft |
| Non Proprietary Name: | sertraline hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; sertraline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zoloft
| Product NDC: | 55154-2709 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019839 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920211 |
Package Information of Zoloft
| Package NDC: | 55154-2709-0 |
| Package Description: | 10 BLISTER PACK in 1 BAG (55154-2709-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Zoloft
| NDC Code | 55154-2709-0 |
| Proprietary Name | Zoloft |
| Package Description | 10 BLISTER PACK in 1 BAG (55154-2709-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 55154-2709 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sertraline hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19920211 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | SERTRALINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
