Paroxetine - 21695-101-30 - (Paroxetine Hydrochloride)

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Drug Information of Paroxetine

Product NDC: 21695-101
Proprietary Name: Paroxetine
Non Proprietary Name: Paroxetine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Paroxetine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Paroxetine

Product NDC: 21695-101
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077584
Marketing Category: ANDA
Start Marketing Date: 20070413

Package Information of Paroxetine

Package NDC: 21695-101-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-101-30)

NDC Information of Paroxetine

NDC Code 21695-101-30
Proprietary Name Paroxetine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-101-30)
Product NDC 21695-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paroxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070413
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Paroxetine


General Information