Paroxetine - 51079-774-20 - (paroxetine hydrochloride hemihydrate)

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Drug Information of Paroxetine

Product NDC: 51079-774
Proprietary Name: Paroxetine
Non Proprietary Name: paroxetine hydrochloride hemihydrate
Active Ingredient(s): 20    mg/1 & nbsp;   paroxetine hydrochloride hemihydrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Paroxetine

Product NDC: 51079-774
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078902
Marketing Category: ANDA
Start Marketing Date: 20120907

Package Information of Paroxetine

Package NDC: 51079-774-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-774-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-774-01)

NDC Information of Paroxetine

NDC Code 51079-774-20
Proprietary Name Paroxetine
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-774-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-774-01)
Product NDC 51079-774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name paroxetine hydrochloride hemihydrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120907
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information