NDC 16714-181 – Paroxetine

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

Human Prescription Drug

Product NDC16714-181

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 (4)

Package NDCDescriptionSince
16714-181-0130 TABLET, FILM COATED in 1 BOTTLE (16714-181-01)Jul 25, 2007
16714-181-0290 TABLET, FILM COATED in 1 BOTTLE (16714-181-02)Jul 25, 2007
16714-181-04500 TABLET, FILM COATED in 1 BOTTLE (16714-181-04)Jul 25, 2007
16714-181-051000 TABLET, FILM COATED in 1 BOTTLE (16714-181-05)Jul 25, 2007

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