Product NDC: | 59762-4940 |
Proprietary Name: | SERTRALINE HYDROCHLORIDE |
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) |
Product NDC: | 59762-4940 |
Labeler Name: | Greenstone LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020990 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 19920211 |
Package NDC: | 59762-4940-1 |
Package Description: | 60 mL in 1 BOTTLE, DROPPER (59762-4940-1) |
NDC Code | 59762-4940-1 |
Proprietary Name | SERTRALINE HYDROCHLORIDE |
Package Description | 60 mL in 1 BOTTLE, DROPPER (59762-4940-1) |
Product NDC | 59762-4940 |
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 AUTHORIZED GENERIC |
Labeler Name | Greenstone LLC |
Substance Name | SERTRALINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |