Prescription drug · ANDA
Sodium Iodide I 123 NDC 69945-601
Sodium iodide i-123 100 uCi/1 · Capsule, Gelatin coated · Oral · Curium US LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69945-601-10 | 6994506011069945060110 | 1 BOTTLE in 1 CAN (69945-601-10) / 1 CAPSULE, GELATIN COATED in 1 BOTTLEMarketed from Nov 4, 2015 |
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 — 100 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 071909
- Marketing start
- Listing expires
- Identifiers
- Product ID 69945-601_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
N469945060110followed by a unit qualifier and the quantityPackage 69945-0601-10. 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.
About NDC 69945-601
- What is NDC 69945-601?
- 69945-601 is the product NDC for Sodium Iodide I 123, Sodium iodide i-123 100 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.
Related NDCs: other Sodium Iodide I 123 products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Sodium Iodide I 123 | Sodium iodide i-123 200 uCi/1 | Capsule, Gelatin coatedOral | Curium US LLC | 69945-602 | 69945-0602-20 |
| Sodium Iodide I 123 | Sodium iodide i-123 100 uCi/1 | Capsule, Gelatin coatedOral | Cardinal Health 418, Inc | 48815-1001 | 48815-1001-0148815-1001-05 |
| Sodium Iodide I 123 | Sodium iodide i-123 200 uCi/1 | Capsule, Gelatin coatedOral | Cardinal Health 418, Inc | 48815-1002 | 48815-1002-0148815-1002-05 |