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Sertraline Hydrochloride - 52125-217-19 - (Sertraline Hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 52125-217
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
Coding System: National Drug Codes(NDC)

Labeler Information of Sertraline Hydrochloride

Product NDC: 52125-217
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077397
Marketing Category: ANDA
Start Marketing Date: 20130327

Package Information of Sertraline Hydrochloride

Package NDC: 52125-217-19
Package Description: 90 TABLET in 1 VIAL (52125-217-19)

NDC Information of Sertraline Hydrochloride

NDC Code 52125-217-19
Proprietary Name Sertraline Hydrochloride
Package Description 90 TABLET in 1 VIAL (52125-217-19)
Product NDC 52125-217
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sertraline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130327
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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