NDC 65862-157 – Paroxetine

Paroxetine Hydrochloride Hemihydrate 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-157

Product details

Brand name
Paroxetine
Generic name
Paroxetine Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078406
Marketed since
July 25, 2007
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
65862-157-01100 TABLET, FILM COATED in 1 BOTTLE (65862-157-01)Jul 25, 2007
65862-157-05500 TABLET, FILM COATED in 1 BOTTLE (65862-157-05)Jul 25, 2007
65862-157-3030 TABLET, FILM COATED in 1 BOTTLE (65862-157-30)Jul 25, 2007
65862-157-9090 TABLET, FILM COATED in 1 BOTTLE (65862-157-90)Jul 25, 2007
65862-157-991000 TABLET, FILM COATED in 1 BOTTLE (65862-157-99)Jul 25, 2007

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