NDC 69584-673 – Paroxetine hydrochloride

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

Human Prescription Drug

Product NDC69584-673

Product details

Brand name
Paroxetine hydrochloride
Generic name
Paroxetine hydrochloride
Labeler
Oxford Pharmaceuticals, LLC
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 (5)

Package NDCDescriptionSince
69584-673-0330 TABLET, FILM COATED in 1 BOTTLE (69584-673-03)Nov 14, 2022
69584-673-0990 TABLET, FILM COATED in 1 BOTTLE (69584-673-09)Nov 14, 2022
69584-673-10100 TABLET, FILM COATED in 1 BOTTLE (69584-673-10)Nov 14, 2022
69584-673-50500 TABLET, FILM COATED in 1 BOTTLE (69584-673-50)Nov 14, 2022
69584-673-901000 TABLET, FILM COATED in 1 BOTTLE (69584-673-90)Nov 14, 2022

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