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SERTRALINE HYDROCHLORIDE - 55154-0527-0 - (sertraline hydrochloride)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 55154-0527
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: 55154-0527
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA
Start Marketing Date: 19920211

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 55154-0527-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0527-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 55154-0527-0
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 10 BLISTER PACK in 1 BAG (55154-0527-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-0527
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19920211
Marketing Category Name NDA
Labeler Name Cardinal Health
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


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