Dehydrated Alcohol (alcohol) NDC 16729-710

NDC codes

FDA NDC Directory

Product NDC (as listed)16729-710Labeler and product segments. Claims need a package NDC.

Product NDC at billing width16729-0710Add 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
16729-710-45	16729071045	10 VIAL in 1 CARTON (16729-710-45) / 5 mL in 1 VIAL (16729-710-31)Marketed from Jun 25, 2025
16729-710-53	16729071053	5 VIAL in 1 CARTON (16729-710-53) / 5 mL in 1 VIAL (16729-710-31)Marketed from Apr 16, 2026

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): Dehydrated Alcohol
Generic name (nonproprietary): alcohol
Active ingredients: Alcohol — 1 mL/mL
Dosage form: Injection, Solution
Route: Percutaneous
Labeler: Accord Healthcare, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217845
Marketing start: Jun 25, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 16729-710_52566f68-6e40-af49-e063-6394a90a01adSPL ID 52566f68-6e40-af49-e063-6394a90a01adSPL set ID 07fa92f7-d752-42e3-a572-b552461c4389RxCUI 2048982UNII 3K9958V90M

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.

NDC on a medical claim

N416729071045 followed by a unit qualifier and the quantity

Package 16729-0710-45. 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 21, 2026.

Indications (excerpt from the label)

Dehydrated alcohol injection is indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy. Dehydrated alcohol injection is an ablative agent indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)