Product NDC: | 16590-251 |
Proprietary Name: | ZOLOFT |
Non Proprietary Name: | SERTRALINE HYDROCHLORIDE |
Active Ingredient(s): | 100 mg/1 & nbsp; SERTRALINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-251 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019839 |
Marketing Category: | NDA |
Start Marketing Date: | 19920211 |
Package NDC: | 16590-251-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (16590-251-60) |
NDC Code | 16590-251-60 |
Proprietary Name | ZOLOFT |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (16590-251-60) |
Product NDC | 16590-251 |
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 | STAT RX USA LLC |
Substance Name | SERTRALINE HYDROCHLORIDE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |