NDC 76420-718 – Paroxetine

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

Human Prescription Drug

Product NDC76420-718

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
April 13, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

Package NDC codes (6)

Package NDCDescriptionSince
76420-718-01100 TABLET, FILM COATED in 1 BOTTLE (76420-718-01)May 6, 2024
76420-718-05500 TABLET, FILM COATED in 1 BOTTLE (76420-718-05)May 6, 2024
76420-718-101000 TABLET, FILM COATED in 1 BOTTLE (76420-718-10)May 6, 2024
76420-718-3030 TABLET, FILM COATED in 1 BOTTLE (76420-718-30)May 6, 2024
76420-718-6060 TABLET, FILM COATED in 1 BOTTLE (76420-718-60)May 6, 2024
76420-718-9090 TABLET, FILM COATED in 1 BOTTLE (76420-718-90)May 6, 2024

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