NDC 68180-978 – Sertraline Hydrochloride

Sertraline Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC68180-978

Product details

Brand name
Sertraline Hydrochloride
Generic name
Sertraline Hydrochloride
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077670
Marketed since
July 20, 2025
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sertraline hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
68180-978-0130 TABLET, FILM COATED in 1 BOTTLE (68180-978-01)Jul 20, 2025
68180-978-0290 TABLET, FILM COATED in 1 BOTTLE (68180-978-02)Jul 20, 2025
68180-978-031000 TABLET, FILM COATED in 1 BOTTLE (68180-978-03)Jul 20, 2025

Recalls mentioning this NDC

Other Sertraline hydrochloride products