NDC 68180-986 – Sertraline Hydrochloride

Sertraline Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC68180-986

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
August 6, 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 (4)

Package NDCDescriptionSince
68180-986-0130 TABLET, FILM COATED in 1 BOTTLE (68180-986-01)Aug 6, 2025
68180-986-0290 TABLET, FILM COATED in 1 BOTTLE (68180-986-02)Aug 6, 2025
68180-986-03500 TABLET, FILM COATED in 1 BOTTLE (68180-986-03)Aug 6, 2025
68180-986-045000 TABLET, FILM COATED in 1 BOTTLE (68180-986-04)Aug 6, 2025

Recalls mentioning this NDC

Other Sertraline hydrochloride products