United States · FDA National Drug Code directory
Fludeoxyglucose F 18
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
- 49609-101_43f8e45a-9c5d-81fa-e063-6394a90acbf4
- Product NDC
- 49609-101
- Form
- INJECTION
- Composition / generic term
- Fludeoxyglucose F-18
- Labeler
- SOFIE Co.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111208
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUDEOXYGLUCOSE F-18 — 300 mCi/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 VIAL, MULTI-DOSE (49609-101-01) · 49609-101-01
- 50 mL in 1 VIAL, MULTI-DOSE (49609-101-02) · 49609-101-02
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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