NDC 68180-647 – Paroxetine

Paroxetine Hydrochloride Hemihydrate 12.5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC68180-647

Product details

Brand name
Paroxetine
Generic name
Paroxetine
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204134
Marketed since
March 6, 2017
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paroxetine →

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