NDC codes

FDA NDC Directory
Product NDC (as listed)51991-999Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51991-0999Add 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
51991-999-17519910999175199109991710 VIAL, GLASS in 1 CARTON (51991-999-17) / 5 mL in 1 VIAL, GLASS (51991-999-75)Marketed from Sep 23, 2025

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
Intra-arterial
Labeler
Breckenridge Pharmaceutical IncNDC labeler code 51991
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 219444
Marketing start
Listing expires
Identifiers
Product ID 51991-999_5329ec90-465f-42c4-ac98-b5f0d644abfaSPL ID 5329ec90-465f-42c4-ac98-b5f0d644abfaSPL set ID be10b253-d72a-4f57-aa27-94c70ae8aed3RxCUI 2048982UNII 3K9958V90MUPC 0351991999171

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

N451991099917 followed by a unit qualifier and the quantity

Package 51991-0999-17. 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)

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)

About NDC 51991-999

What is NDC 51991-999?
51991-999 is the product NDC for Dehydrated Alcohol (alcohol), Alcohol 1 mL/mL injection, solution, listed with the FDA by Breckenridge Pharmaceutical Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dehydrated Alcohol (Alcohol).
What is the active ingredient?
Alcohol.
Who is the labeler?
Breckenridge Pharmaceutical Inc, NDC labeler code 51991. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dehydrated Alcohol?
9 other product NDCs are listed under this name. See all Dehydrated Alcohol 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 Dehydrated Alcohol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousAjenat Pharmaceuticals LLC82983-42682983-0426-10
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousAvenacy, LLC83634-30683634-0306-0583634-0306-06
Dehydrated AlcoholDehydrated alcohol 5 mL/5mLInjection, SolutionPercutaneousIngenus Pharmaceuticals, LLC50742-53950742-0539-10
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousAccord Healthcare, Inc.16729-71016729-0710-4516729-0710-53
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousXGen Pharmaceuticals DJB, Inc.39822-930039822-9300-02
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousA-S Medication Solutions50090-764350090-7643-0050090-7643-01
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousBPI Labs, LLC54288-14454288-0144-10
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjectionPercutaneousSolupharm Pharmazeutische Erzeugnisse GmbH55579-30655579-0306-0555579-0306-41
Dehydrated AlcoholalcoholAlcohol 1 mL/mLInjection, SolutionPercutaneousBPI Labs, LLC54288-10554288-0105-1054288-0105-15

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