NDC 16714-182 – Paroxetine

Paroxetine Hydrochloride Hemihydrate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC16714-182

Product details

Brand name
Paroxetine
Generic name
Paroxetine Hydrochloride
Labeler
NorthStar Rx LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078406
Marketed since
July 25, 2007
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (3)

Package NDCDescriptionSince
16714-182-0130 TABLET, FILM COATED in 1 BOTTLE (16714-182-01)Jul 25, 2007
16714-182-03100 TABLET, FILM COATED in 1 BOTTLE (16714-182-03)Jul 25, 2007
16714-182-041000 TABLET, FILM COATED in 1 BOTTLE (16714-182-04)Jul 25, 2007

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