What is NDC 51662-1562?

51662-1562 is the product NDC for Sodium Tetradecyl Sulfate, Tetradecyl hydrogen sulfate (Ester) 10 mg/mL injection, solution, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Tetradecyl hydrogen sulfate (Ester).

HF Acquisition Co LLC, DBA HealthFirst, NDC labeler code 51662. 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 Tetradecyl Sulfate?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium Tetradecyl Sulfate NDC 51662-1562

NDC codes

FDA NDC Directory

Product NDC (as listed)51662-1562Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51662-1562Add 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
51662-1562-1	51662156201	2 mL in 1 VIAL, MULTI-DOSE (51662-1562-1)Marketed from Jul 18, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 Tetradecyl Sulfate
Generic name (nonproprietary): sodium tetradecyl sulfate
Active ingredients: Tetradecyl hydrogen sulfate (Ester) — 10 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: HF Acquisition Co LLC, DBA HealthFirstNDC labeler code 51662
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040541
Marketing start: Jul 18, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 51662-1562_1203bbfe-c55f-1bcb-e063-6394a90a6577SPL ID 1203bbfe-c55f-1bcb-e063-6394a90a6577SPL set ID c76f4b3b-9f93-349f-e053-2995a90a2d57RxCUI 204490UNII 6326W0DRHY

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

N451662156201 followed by a unit qualifier and the quantity

Package 51662-1562-01. 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 Feb 22, 2024.

Indications (excerpt from the label)

INDICATIONS & USAGE Sotradecol (sodium tetradecyl sulfate injection) is indicated in the treatment of small uncomplicated varicose veins of the lower extremities that show simple dilation with competent valves. The benefit-to-risk ratio should be considered in selected patients who are great surgical risks.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51662-1562

What is NDC 51662-1562?: 51662-1562 is the product NDC for Sodium Tetradecyl Sulfate, Tetradecyl hydrogen sulfate (Ester) 10 mg/mL injection, solution, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sodium Tetradecyl Sulfate.
What is the active ingredient?: Tetradecyl hydrogen sulfate (Ester).
Who is the labeler?: HF Acquisition Co LLC, DBA HealthFirst, NDC labeler code 51662. 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 Tetradecyl Sulfate?: 1 other product NDC are listed under this name. See all Sodium Tetradecyl Sulfate 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 Tetradecyl Sulfate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sodium Tetradecyl Sulfate	Sodium tetradecyl sulfate 30 mg/mL	Injection, SolutionIntravenous	Hikma Pharmaceuticals USA Inc.	24201-201	24201-0201-05

Other NDCs under ANDA 040541

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

FDA NDC Directory listings under ANDA 040541
Product	Strength	Form · route	Labeler	Product NDC
(Sotradecol) Sodium Tetradecyl Sulfate	Tetradecyl hydrogen sulfate (Ester) 30 mg/mL	Injection, SolutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1563
Sotradecoltetradecyl hydrogen sulfate (ester)	Tetradecyl hydrogen sulfate (Ester) 10 mg/mL	Injection, SolutionIntravenous	Mylan Institutional LLC	67457-162
Sotradecoltetradecyl hydrogen sulfate (ester)	Tetradecyl hydrogen sulfate (Ester) 30 mg/mL	Injection, SolutionIntravenous	Mylan Institutional LLC	67457-163