NDC codes

FDA NDC Directory
Product NDC (as listed)69945-602Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69945-0602Add 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 NDC11-digit (billing)PackageCopy
69945-602-2069945060220699450602201 BOTTLE in 1 CAN (69945-602-20) / 1 CAPSULE, GELATIN COATED in 1 BOTTLEMarketed from Apr 11, 2007

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 Iodide I 123
Generic name (nonproprietary)
sodium iodide i 123
Active ingredients
Sodium iodide i-123 — 200 uCi/1
Dosage form
Capsule, Gelatin coated
Route
Oral
Labeler
Curium US LLCNDC labeler code 69945
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071910
Marketing start
Listing expires
Identifiers
Product ID 69945-602_24b19127-9a67-0ddf-e063-6394a90ae0b5SPL ID 24b19127-9a67-0ddf-e063-6394a90ae0b5SPL set ID 493fa2ab-4eb0-4434-9739-3079b2f0e272UNII 29UKX3A616

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N469945060220 followed by a unit qualifier and the quantity

Package 69945-0602-20. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Administration of Sodium Iodide I 123 Capsules is indicated as a diagnostic procedure to be used in evaluating thyroid function and/or morphology.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69945-602

What is NDC 69945-602?
69945-602 is the product NDC for Sodium Iodide I 123, Sodium iodide i-123 200 uCi/1 capsule, gelatin coated, listed with the FDA by Curium US LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sodium Iodide I 123.
What is the active ingredient?
Sodium iodide i-123.
Who is the labeler?
Curium US LLC, NDC labeler code 69945. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sodium Iodide I 123?
3 other product NDCs are listed under this name. See all Sodium Iodide I 123 NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sodium Iodide I 123 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sodium Iodide I 123Sodium iodide i-123 100 uCi/1Capsule, Gelatin coatedOralCurium US LLC69945-60169945-0601-10
Sodium Iodide I 123Sodium iodide i-123 100 uCi/1Capsule, Gelatin coatedOralCardinal Health 418, Inc48815-100148815-1001-0148815-1001-05
Sodium Iodide I 123Sodium iodide i-123 200 uCi/1Capsule, Gelatin coatedOralCardinal Health 418, Inc48815-100248815-1002-0148815-1002-05

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