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Sertraline Hydrochloride - 51138-587-30 - (sertraline hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 51138-587
Proprietary Name: Sertraline Hydrochloride
Non Proprietary Name: sertraline hydrochloride
Active Ingredient(s): 100    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: 51138-587
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077864
Marketing Category: ANDA
Start Marketing Date: 20110704

Package Information of Sertraline Hydrochloride

Package NDC: 51138-587-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-587-30)

NDC Information of Sertraline Hydrochloride

NDC Code 51138-587-30
Proprietary Name Sertraline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-587-30)
Product NDC 51138-587
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110704
Marketing Category Name ANDA
Labeler Name Med-Health Pharma, LLC
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Sertraline Hydrochloride


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