NDC 68788-6870 – Paroxetine

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

Human Prescription Drug

Product NDC68788-6870

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
January 11, 2017
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
68788-6870-1100 TABLET, FILM COATED in 1 BOTTLE (68788-6870-1)Jan 11, 2017
68788-6870-330 TABLET, FILM COATED in 1 BOTTLE (68788-6870-3)Jan 11, 2017
68788-6870-660 TABLET, FILM COATED in 1 BOTTLE (68788-6870-6)Jan 11, 2017
68788-6870-8120 TABLET, FILM COATED in 1 BOTTLE (68788-6870-8)Jan 11, 2017
68788-6870-990 TABLET, FILM COATED in 1 BOTTLE (68788-6870-9)Jan 11, 2017

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