# Sodium Fluoride F 18

NDC: 76451-018
Generic name: SODIUM FLUORIDE F-18
Labeler / Manufacturer: 3D Imaging Drug Design and Development LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20120102

FDA application: ANDA203777

## 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:"76451-018"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76451-018
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eeaf4f42-e3c6-4e0a-aa79-89722511eaea