Sodium Fluoride F 18 (sodium fluoride f-18) NDC 81759-002

NDC codes

FDA NDC Directory

Product NDC (as listed)81759-002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width81759-0002Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
81759-002-30	81759000230	1 VIAL, GLASS in 1 CONTAINER (81759-002-30) / 10 mL in 1 VIAL, GLASSMarketed from Dec 6, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Sodium Fluoride F 18Suffix: F 18
Generic name (nonproprietary): sodium fluoride f-18
Active ingredients: Sodium fluoride f-18 — 200 mCi/mL
Dosage form: Injection
Route: Intravenous
Labeler: BAMF Health Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204328
Marketing start: Dec 6, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Radiopharmaceutical Activity (Mechanism)
Identifiers: Product ID 81759-002_0da6e293-9150-3146-e063-6394a90a0399SPL ID 0da6e293-9150-3146-e063-6394a90a0399SPL set ID ef58c3cd-a922-c5fc-e053-2a95a90a9d74UNII 9L75099X6R
Pharmacologic class: Radioactive Diagnostic Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N481759000230 followed by a unit qualifier and the quantity

Package 81759-0002-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 29, 2023.

Indications (excerpt from the label)

Sodium Fluoride F 18 Injection is indicated for diagnostic positron emission tomography (PET) imaging of bone to define areas of altered osteogenic activity. Sodium Fluoride F 18 Injection is a radioactive diagnostic agent for positron emission tomography (PET) indicated for imaging of bone to define areas of altered osteogenic activity.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204328

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 204328
Product	Strength	Form · route	Labeler	Product NDC
Sodium Fluoride F 18	Sodium fluoride f-18 600 mCi/mL	InjectionIntravenous	THE FEINSTEIN INSTITUTES FOR MEDICAL RESEARCH	13267-542