NDC 13107-154 – Paroxetine

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

Human Prescription Drug

Product NDC13107-154

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Aurolife Pharma LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078406
Marketed since
December 3, 2009
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (5)

Package NDCDescriptionSince
13107-154-01100 TABLET, FILM COATED in 1 BOTTLE (13107-154-01)Dec 3, 2009
13107-154-05500 TABLET, FILM COATED in 1 BOTTLE (13107-154-05)Dec 3, 2009
13107-154-3030 TABLET, FILM COATED in 1 BOTTLE (13107-154-30)Dec 3, 2009
13107-154-9090 TABLET, FILM COATED in 1 BOTTLE (13107-154-90)Dec 3, 2009
13107-154-991000 TABLET, FILM COATED in 1 BOTTLE (13107-154-99)Dec 3, 2009

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