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Sertraline Hydrochloride - 51079-762-20 - (sertraline hydrochloride)

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Drug Information of Sertraline Hydrochloride

Product NDC: 51079-762
Proprietary Name: Sertraline Hydrochloride
Non Proprietary Name: sertraline hydrochloride
Active Ingredient(s): 25    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: 51079-762
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076671
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of Sertraline Hydrochloride

Package NDC: 51079-762-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-762-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-762-01)

NDC Information of Sertraline Hydrochloride

NDC Code 51079-762-20
Proprietary Name Sertraline Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-762-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-762-01)
Product NDC 51079-762
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sertraline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name SERTRALINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Sertraline Hydrochloride


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