NDC 70518-3518 – Paroxetine

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

Human Prescription Drug

Product NDC70518-3518

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077584
Marketed since
September 13, 2022
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
70518-3518-0100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-0)Sep 13, 2022
70518-3518-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-3518-1)Sep 29, 2022
70518-3518-2100 POUCH in 1 BOX (70518-3518-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3518-3)Jan 31, 2025
70518-3518-430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-4)Jun 18, 2025
70518-3518-645 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-6)Apr 16, 2026

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