Paroxetine

Product NDC
55154-5087
11-digit product format
551545087
Labeler code
55154
Product ID
55154-5087_639297f7-99af-416e-89e3-2abfcdb55abe
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Paroxetine hydrochloride hemihydrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Cardinal Health
Application
ANDA078902
Marketing category
ANDA
Marketing start
2011-01-14
Marketing end
2020-10-31
Substance
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Active strength
20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
X2ELS050D8PAROXETINE HYDROCHLORIDE HEMIHYDRATE110429-35-1PAROXETINE HYDROCHLORIDE HEMIHYDRATE