NDC 68382-001 – Paroxetine

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

Human Prescription Drug 2 recalls

Product NDC68382-001

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Zydus Pharmaceuticals USA Inc.
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 (5)

Package NDCDescriptionSince
68382-001-01100 TABLET, FILM COATED in 1 BOTTLE (68382-001-01)Apr 13, 2007
68382-001-05500 TABLET, FILM COATED in 1 BOTTLE (68382-001-05)Apr 13, 2007
68382-001-0630 TABLET, FILM COATED in 1 BOTTLE (68382-001-06)Apr 13, 2007
68382-001-101000 TABLET, FILM COATED in 1 BOTTLE (68382-001-10)Apr 13, 2007
68382-001-1690 TABLET, FILM COATED in 1 BOTTLE (68382-001-16)Apr 13, 2007

Recalls mentioning this NDC

Other Paroxetine products