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SERTRALINE HYDROCHLORIDE - 59762-4900-4 - (SERTRALINE HYDROCHLORIDE)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 59762-4900
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)

Labeler Information of SERTRALINE HYDROCHLORIDE

Product NDC: 59762-4900
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: 59762-4900-4
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (59762-4900-4)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 59762-4900-4
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (59762-4900-4)
Product NDC 59762-4900
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 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of SERTRALINE HYDROCHLORIDE


General Information