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Sertraline Hydrochloride Tablets - 0904-6089-61 - (sertraline hydrochloride)

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Drug Information of Sertraline Hydrochloride Tablets

Product NDC: 0904-6089
Proprietary Name: Sertraline Hydrochloride Tablets
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 Tablets

Product NDC: 0904-6089
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077397
Marketing Category: ANDA
Start Marketing Date: 20091110

Package Information of Sertraline Hydrochloride Tablets

Package NDC: 0904-6089-61
Package Description: 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6089-61)

NDC Information of Sertraline Hydrochloride Tablets

NDC Code 0904-6089-61
Proprietary Name Sertraline Hydrochloride Tablets
Package Description 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6089-61)
Product NDC 0904-6089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091110
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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 Tablets


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