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Paroxetine Hydrochloride - 49349-364-02 - (Paroxetine Hydrochloride)

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Drug Information of Paroxetine Hydrochloride

Product NDC: 49349-364
Proprietary Name: Paroxetine Hydrochloride
Non Proprietary Name: Paroxetine Hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   Paroxetine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Paroxetine Hydrochloride

Product NDC: 49349-364
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20110711

Package Information of Paroxetine Hydrochloride

Package NDC: 49349-364-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-364-02)

NDC Information of Paroxetine Hydrochloride

NDC Code 49349-364-02
Proprietary Name Paroxetine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-364-02)
Product NDC 49349-364
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110711
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine Hydrochloride


General Information