NDC 71335-0544 – Paroxetine

Paroxetine Hydrochloride Hemihydrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0544

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 (7)

Package NDCDescriptionSince
71335-0544-130 TABLET, FILM COATED in 1 BOTTLE (71335-0544-1)Feb 9, 2022
71335-0544-260 TABLET, FILM COATED in 1 BOTTLE (71335-0544-2)Feb 9, 2022
71335-0544-390 TABLET, FILM COATED in 1 BOTTLE (71335-0544-3)Feb 9, 2022
71335-0544-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0544-4)Feb 9, 2022
71335-0544-515 TABLET, FILM COATED in 1 BOTTLE (71335-0544-5)Feb 9, 2022
71335-0544-620 TABLET, FILM COATED in 1 BOTTLE (71335-0544-6)Feb 9, 2022
71335-0544-7180 TABLET, FILM COATED in 1 BOTTLE (71335-0544-7)Feb 9, 2022

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