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Sertraline Hydrochloride Tablets
Sertraline Hydrochloride Tablets - 0904-6088-61 - (sertraline hydrochloride)
Drug Information of Sertraline Hydrochloride Tablets
| Product NDC: | 0904-6088 |
| Proprietary Name: | Sertraline Hydrochloride Tablets |
| 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) |
Labeler Information of Sertraline Hydrochloride Tablets
| Product NDC: | 0904-6088 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077397 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091110 |
Package Information of Sertraline Hydrochloride Tablets
| Package NDC: | 0904-6088-61 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6088-61) |
NDC Information of Sertraline Hydrochloride Tablets
| NDC Code | 0904-6088-61 |
| Proprietary Name | Sertraline Hydrochloride Tablets |
| Package Description | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6088-61) |
| Product NDC | 0904-6088 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sertraline hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091110 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | SERTRALINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
