ZOLOFT - 49999-292-30 - (SERTRALINE HYDROCHLORIDE)

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Drug Information of ZOLOFT

Product NDC: 49999-292
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: 49999-292
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA
Start Marketing Date: 20120403

Package Information of ZOLOFT

Package NDC: 49999-292-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (49999-292-30)

NDC Information of ZOLOFT

NDC Code 49999-292-30
Proprietary Name ZOLOFT
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (49999-292-30)
Product NDC 49999-292
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SERTRALINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120403
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products 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 ZOLOFT


General Information