Paroxetine

Product NDC
52343-073
11-digit product format
523430073
Labeler code
52343
Product ID
52343-073_1a57b09e-842c-4f1b-91ca-03f0be9fe767
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Paroxetine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ACETRIS HEALTH, LLC
Application
ANDA078406
Marketing category
ANDA
Marketing start
2007-07-25
Marketing end
2021-02-01
Substance
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Active strength
10 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52343-073-30EA - Each52343-0736bd63ade-abc5-42b5-bddf-90a7e155953d12015-01-05
52343-073-90EA - Each52343-073f5bfc4f2-1676-47fd-83b1-f1177531bc9b12015-01-05
52343-073-99EA - Each52343-073351ce44b-1487-48d0-a768-3aadcae66a3412015-01-05