# Sodium Fluoride F 18

NDC: 49609-102
Generic name: SODIUM FLUORIDE F-18
Labeler / Manufacturer: SOFIE Co.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20111208

FDA application: ANDA203592

## Active ingredients

- SODIUM FLUORIDE F-18: 200 mCi/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49609-102"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49609-102
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2bbd8f48-fdf9-45cb-8305-124a03f7a52c