NDC 80425-0339 – Paroxetine

Paroxetine Hydrochloride Hemihydrate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC80425-0339

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
May 19, 2023
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0339-130 TABLET, FILM COATED in 1 BOTTLE (80425-0339-1)May 19, 2023
80425-0339-260 TABLET, FILM COATED in 1 BOTTLE (80425-0339-2)May 19, 2023
80425-0339-390 TABLET, FILM COATED in 1 BOTTLE (80425-0339-3)May 19, 2023

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