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SERTRALINE HYDROCHLORIDE - 35356-033-30 - (SERTRALINE HYDROCHLORIDE)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 35356-033
Proprietary Name: SERTRALINE HYDROCHLORIDE
Non Proprietary Name: SERTRALINE HYDROCHLORIDE
Active Ingredient(s): 25    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: 35356-033
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: 20111219

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 35356-033-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (35356-033-30)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 35356-033-30
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (35356-033-30)
Product NDC 35356-033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SERTRALINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111219
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of SERTRALINE HYDROCHLORIDE


General Information