United States · FDA National Drug Code directory
SERTRALINE HYDROCHLORIDE
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
- 71335-0415_b77be777-f7b7-4f83-ad5e-2dca97a8b2a2
- Product NDC
- 71335-0415
- Form
- TABLET, FILM COATED
- Composition / generic term
- SERTRALINE HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170209
- Source listing expiry
- 20261231
Source-listed ingredients
- SERTRALINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0415-1) · 71335-0415-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0415-2) · 71335-0415-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0415-3) · 71335-0415-3
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-0415-4) · 71335-0415-4
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-0415-5) · 71335-0415-5
- 56 TABLET, FILM COATED in 1 BOTTLE (71335-0415-6) · 71335-0415-6
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-0415-7) · 71335-0415-7
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0415-8) · 71335-0415-8
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-0415-9) · 71335-0415-9
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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