NDC 58151-576 – Zoloft

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

Human Prescription Drug

Product NDC58151-576

Product details

Brand name
Zoloft
Generic name
Sertraline hydrochloride
Labeler
Viatris Specialty LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA019839
Marketed since
October 30, 2024
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Zoloft →

Package NDC codes (2)

Package NDCDescriptionSince
58151-576-88100 BLISTER PACK in 1 CARTON (58151-576-88) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58151-576-32)Jul 1, 2025
58151-576-9330 TABLET, FILM COATED in 1 BOTTLE (58151-576-93)Nov 26, 2024

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