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
- 71610-886_30b94d78-0158-ff43-e063-6294a90a030b
- Product NDC
- 71610-886
- Form
- TABLET
- Composition / generic term
- Sertraline Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160721
- Source listing expiry
- 20261231
Source-listed ingredients
- SERTRALINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (71610-886-15) · 71610-886-15
- 45 TABLET in 1 BOTTLE (71610-886-45) · 71610-886-45
- 90 TABLET in 1 BOTTLE (71610-886-60) · 71610-886-60
- 135 TABLET in 1 BOTTLE (71610-886-73) · 71610-886-73
- 180 TABLET in 1 BOTTLE (71610-886-80) · 71610-886-80
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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