NDC 71335-0321 – Paroxetine

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

Human Prescription Drug

Product NDC71335-0321

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
April 13, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (4)

Package NDCDescriptionSince
71335-0321-130 TABLET, FILM COATED in 1 BOTTLE (71335-0321-1)Feb 12, 2018
71335-0321-260 TABLET, FILM COATED in 1 BOTTLE (71335-0321-2)Dec 27, 2021
71335-0321-390 TABLET, FILM COATED in 1 BOTTLE (71335-0321-3)May 17, 2018
71335-0321-4180 TABLET, FILM COATED in 1 BOTTLE (71335-0321-4)Dec 27, 2021

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