NDC 71335-9650 – Paroxetine hydrochloride

Paroxetine Hydrochloride Hemihydrate 30 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9650

Product details

Brand name
Paroxetine hydrochloride
Generic name
Paroxetine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076968
Marketed since
November 14, 2022
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
71335-9650-130 TABLET, FILM COATED in 1 BOTTLE (71335-9650-1)Mar 28, 2023
71335-9650-260 TABLET, FILM COATED in 1 BOTTLE (71335-9650-2)Sep 6, 2024
71335-9650-390 TABLET, FILM COATED in 1 BOTTLE (71335-9650-3)Sep 6, 2024
71335-9650-4180 TABLET, FILM COATED in 1 BOTTLE (71335-9650-4)Sep 6, 2024

Other Paroxetine Hydrochloride products