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SERTRALINE HYDROCHLORIDE - 43063-213-01 - (sertraline hydrochloride)

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Drug Information of SERTRALINE HYDROCHLORIDE

Product NDC: 43063-213
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: 43063-213
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019839
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19920211

Package Information of SERTRALINE HYDROCHLORIDE

Package NDC: 43063-213-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-213-01)

NDC Information of SERTRALINE HYDROCHLORIDE

NDC Code 43063-213-01
Proprietary Name SERTRALINE HYDROCHLORIDE
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-213-01)
Product NDC 43063-213
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 AUTHORIZED GENERIC
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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