paroxetine - 53808-0753-1 - (PAROXETINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of paroxetine

Product NDC: 53808-0753
Proprietary Name: paroxetine
Non Proprietary Name: PAROXETINE HYDROCHLORIDE
Active Ingredient(s): 30    mg/1 & nbsp;   PAROXETINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of paroxetine

Product NDC: 53808-0753
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075356
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of paroxetine

Package NDC: 53808-0753-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0753-1)

NDC Information of paroxetine

NDC Code 53808-0753-1
Proprietary Name paroxetine
Package Description 30 TABLET in 1 BLISTER PACK (53808-0753-1)
Product NDC 53808-0753
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PAROXETINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name PAROXETINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of paroxetine


General Information