Zoloft - 0049-4900-30 - (SERTRALINE HYDROCHLORIDE)

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Drug Information of Zoloft

Product NDC: 0049-4900
Proprietary Name: Zoloft
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 Zoloft

Product NDC: 0049-4900
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA
Start Marketing Date: 19920211

Package Information of Zoloft

Package NDC: 0049-4900-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0049-4900-30)

NDC Information of Zoloft

NDC Code 0049-4900-30
Proprietary Name Zoloft
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0049-4900-30)
Product NDC 0049-4900
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
Labeler Name Roerig
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Zoloft


General Information