NDC 68788-9074 – Paroxetine

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

Human Prescription Drug

Product NDC68788-9074

Product details

Brand name
Paroxetine
Generic name
Paroxetine Hydrochloride
Labeler
Preferred Pharmaceuticals, Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
April 13, 2007
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (5)

Package NDCDescriptionSince
68788-9074-1100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-1)Apr 13, 2007
68788-9074-330 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-3)Apr 13, 2007
68788-9074-660 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-6)Apr 13, 2007
68788-9074-8120 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-8)Apr 13, 2007
68788-9074-990 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-9)Apr 13, 2007

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