United States · FDA National Drug Code directory
Gemcitabine
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
- 67457-616_93d514c4-a877-475d-91e0-9cfb232d55ca
- Product NDC
- 67457-616
- Form
- INJECTION, SOLUTION
- Composition / generic term
- GEMCITABINE HYDROCHLORIDE
- Labeler
- Mylan Institutional LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180103
- Source listing expiry
- 20261231
Source-listed ingredients
- GEMCITABINE HYDROCHLORIDE — 200 mg/5.26mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (67457-616-10) / 5.26 mL in 1 VIAL, SINGLE-DOSE · 67457-616-10
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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