Home
>
National Drug Code (NDC)
>
Zoloft
Zoloft - 0049-4940-23 - (SERTRALINE HYDROCHLORIDE)
Drug Information of Zoloft
| Product NDC: | 0049-4940 |
| Proprietary Name: | Zoloft |
| Non Proprietary Name: | SERTRALINE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/mL & nbsp; SERTRALINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zoloft
| Product NDC: | 0049-4940 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020990 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920211 |
Package Information of Zoloft
| Package NDC: | 0049-4940-23 |
| Package Description: | 60 mL in 1 BOTTLE, DROPPER (0049-4940-23) |
NDC Information of Zoloft
| NDC Code | 0049-4940-23 |
| Proprietary Name | Zoloft |
| Package Description | 60 mL in 1 BOTTLE, DROPPER (0049-4940-23) |
| Product NDC | 0049-4940 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SERTRALINE HYDROCHLORIDE |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 19920211 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | SERTRALINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
