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SERTRALINE
SERTRALINE - 76282-213-90 - (Sertraline)
Drug Information of SERTRALINE
| Product NDC: | 76282-213 |
| Proprietary Name: | SERTRALINE |
| Non Proprietary Name: | Sertraline |
| Active Ingredient(s): | 50 mg/1 & nbsp; Sertraline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SERTRALINE
| Product NDC: | 76282-213 |
| Labeler Name: | Exelan Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077397 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120820 |
Package Information of SERTRALINE
| Package NDC: | 76282-213-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (76282-213-90) |
NDC Information of SERTRALINE
| NDC Code | 76282-213-90 |
| Proprietary Name | SERTRALINE |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (76282-213-90) |
| Product NDC | 76282-213 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sertraline |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120820 |
| Marketing Category Name | ANDA |
| Labeler Name | Exelan Pharmaceuticals, Inc. |
| Substance Name | SERTRALINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
