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
- 69097-834_c8cfa2ad-1ee9-4762-8a3e-f3c2df00cee8
- Product NDC
- 69097-834
- Form
- TABLET
- Composition / generic term
- Sertraline Hydrochloride
- Labeler
- Cipla USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160721
- Source listing expiry
- 20271231
Source-listed ingredients
- SERTRALINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (69097-834-02) · 69097-834-02
- 90 TABLET in 1 BOTTLE (69097-834-05) · 69097-834-05
- 100 TABLET in 1 BOTTLE (69097-834-07) · 69097-834-07
- 500 TABLET in 1 BOTTLE (69097-834-12) · 69097-834-12
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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