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SERTRALINE HYDROCHLORIDE
SERTRALINE HYDROCHLORIDE - 59762-4910-2 - (SERTRALINE HYDROCHLORIDE)
Drug Information of SERTRALINE HYDROCHLORIDE
| Product NDC: | 59762-4910 |
| Proprietary Name: | SERTRALINE HYDROCHLORIDE |
| 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) |
Labeler Information of SERTRALINE HYDROCHLORIDE
| Product NDC: | 59762-4910 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019839 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19920211 |
Package Information of SERTRALINE HYDROCHLORIDE
| Package NDC: | 59762-4910-2 |
| Package Description: | 5000 TABLET, FILM COATED in 1 BOTTLE (59762-4910-2) |
NDC Information of SERTRALINE HYDROCHLORIDE
| NDC Code | 59762-4910-2 |
| Proprietary Name | SERTRALINE HYDROCHLORIDE |
| Package Description | 5000 TABLET, FILM COATED in 1 BOTTLE (59762-4910-2) |
| Product NDC | 59762-4910 |
| 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 AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | SERTRALINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
