What is NDC 60267-705?

60267-705 is the product NDC for Sodium Thiosulfate, Sodium thiosulfate 250 mg/mL injection, solution, listed with the FDA by Hope Pharmaceuticals. It has 1 package NDC, shown above in 10- and 11-digit form.

Hope Pharmaceuticals, NDC labeler code 60267. 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 Thiosulfate?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium Thiosulfate NDC 60267-705 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60267-705Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60267-0705Add 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
60267-705-50	60267070550	50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50)Marketed from Feb 14, 2012

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 Thiosulfate
Generic name (nonproprietary): sodium thiosulfate
Active ingredients: Sodium thiosulfate — 250 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Hope PharmaceuticalsNDC labeler code 60267
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 203923
Marketing start: Feb 14, 2012
Listing expires: Dec 31, 2027
Identifiers: Product ID 60267-705_4c4f587f-fb6f-4ce3-a09e-2a6a589b4d2bSPL ID 4c4f587f-fb6f-4ce3-a09e-2a6a589b4d2bSPL set ID 82f55408-2de9-463d-85e8-b39c3b259f0bRxCUI 237832UNII HX1032V43M

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

N460267070550 followed by a unit qualifier and the quantity

Package 60267-0705-50. 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 May 26, 2026.

Indications (excerpt from the label)

Sodium Thiosulfate Injection is indicated for sequential use with sodium nitrite for the treatment of acute cyanide poisoning that is judged to be serious or life-threatening. When the diagnosis of cyanide poisoning is uncertain, the potential risks associated with Sodium Thiosulfate Injection should be carefully weighed against the potential benefits, especially if the patient is not in extremis. Sodium Thiosulfate Injection, an antidote, is indicated for sequential use with sodium nitrite for treatment of acute cyanide poisoning that is judged to be serious or life-threatening. ( 1 ) Use with caution if the diagnosis of cyanide poisoning is uncertain. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60267-705

What is NDC 60267-705?: 60267-705 is the product NDC for Sodium Thiosulfate, Sodium thiosulfate 250 mg/mL injection, solution, listed with the FDA by Hope Pharmaceuticals. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sodium Thiosulfate.
What is the active ingredient?: Sodium thiosulfate.
Who is the labeler?: Hope Pharmaceuticals, NDC labeler code 60267. 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 Thiosulfate?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.