United States · FDA National Drug Code directory
Latanoprost
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
- 25021-001_8ce78c02-d0b0-4629-b51d-0c674c6e2e43
- Product NDC
- 25021-001
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Latanoprost
- Labeler
- Sagent Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250715
- Source listing expiry
- 20261231
Source-listed ingredients
- LATANOPROST — 50 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (25021-001-02) / 2.5 mL in 1 BOTTLE · 25021-001-02
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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