Product NDC: | 54868-5639 |
Proprietary Name: | SERTRALINE HYDROCHLORIDE |
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) |
Product NDC: | 54868-5639 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019839 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20060824 |
Package NDC: | 54868-5639-4 |
Package Description: | 15 TABLET, FILM COATED in 1 BOTTLE (54868-5639-4) |
NDC Code | 54868-5639-4 |
Proprietary Name | SERTRALINE HYDROCHLORIDE |
Package Description | 15 TABLET, FILM COATED in 1 BOTTLE (54868-5639-4) |
Product NDC | 54868-5639 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sertraline hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20060824 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | SERTRALINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |