NDC 68788-8669 – Sertraline

Sertraline Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-8669

Product details

Brand name
Sertraline
Generic name
Sertraline
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077670
Marketed since
May 20, 2024
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sertraline →

Package NDC codes (6)

Package NDCDescriptionSince
68788-8669-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8669-1)May 20, 2024
68788-8669-228 TABLET, FILM COATED in 1 BOTTLE (68788-8669-2)May 20, 2024
68788-8669-330 TABLET, FILM COATED in 1 BOTTLE (68788-8669-3)May 20, 2024
68788-8669-660 TABLET, FILM COATED in 1 BOTTLE (68788-8669-6)May 20, 2024
68788-8669-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8669-8)May 20, 2024
68788-8669-990 TABLET, FILM COATED in 1 BOTTLE (68788-8669-9)May 20, 2024

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