United States · FDA National Drug Code directory
ganciclovir
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
- 25021-185_696f706f-39d7-4647-a506-2ebf7b956cc1
- Product NDC
- 25021-185
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ganciclovir sodium
- Labeler
- Sagent Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180215
- Source listing expiry
- 20261231
Source-listed ingredients
- GANCICLOVIR SODIUM — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (25021-185-10) / 10 mL in 1 VIAL · 25021-185-10
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →