United States · FDA National Drug Code directory
Zoloft
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 58151-575_fd27d2f5-1ade-4dbf-b2d2-bb98daf7da3a
- Product NDC
- 58151-575
- Form
- TABLET, FILM COATED
- Composition / generic term
- sertraline hydrochloride
- Labeler
- Viatris Specialty LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20250708
- Source listing expiry
- 20261231
Source-listed ingredients
- SERTRALINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (58151-575-88) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58151-575-32) · 58151-575-88
- 30 TABLET, FILM COATED in 1 BOTTLE (58151-575-93) · 58151-575-93
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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