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SERTRALINE HYDROCHLORIDE - 49999-860-60 - (SERTRALINE HYDROCHLORIDE)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 49999-860
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: 49999-860
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111107

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 49999-860-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (49999-860-60)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 49999-860-60
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (49999-860-60)
Product NDC 49999-860
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SERTRALINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111107
Marketing Category Name NDA AUTHORIZED GENERIC
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 SERTRALINE HYDROCHLORIDE


General Information