# Sodium Fluoride F 18

NDC: 62072-500
Generic name: SODIUM FLUORIDE F-18
Labeler / Manufacturer: Kreitchman PET Center
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20160523

FDA application: ANDA203936

## 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:"62072-500"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62072-500
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df1389d2-1b9b-4327-856e-5ba38118d389