NDC 68084-046 – Paroxetine

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

Human Prescription Drug 1 recall

Product NDC68084-046

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
March 15, 2005
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (1)

Package NDCDescriptionSince
68084-046-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-046-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-046-11)Mar 15, 2005

Recalls mentioning this NDC

Other Paroxetine products