NDC codes

FDA NDC Directory
Product NDC (as listed)51662-1444Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51662-1444Add 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
51662-1444-1516621444015166214440110 mL in 1 VIAL, SINGLE-DOSE (51662-1444-1)Marketed from Dec 22, 2019
51662-1444-3516621444035166214440325 POUCH in 1 CASE (51662-1444-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1444-2) / 10 mL in 1 VIAL, SINGLE-DOSEMarketed from Sep 12, 2022

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)
Esmolol Hydrochloride
Generic name (nonproprietary)
esmolol hydrochloride
Active ingredients
Esmolol hydrochloride — 100 mg/10mL
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 205520
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 51662-1444_101e0203-54eb-a48a-e063-6294a90af0d0SPL ID 101e0203-54eb-a48a-e063-6294a90af0d0SPL set ID 9a52d2fd-e551-f8f1-e053-2995a90a6c09RxCUI 1736546UNII V05260LC8D
Pharmacologic class
beta-Adrenergic Blocker

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

N451662144401 followed by a unit qualifier and the quantity

Package 51662-1444-01. 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 .

Indications (excerpt from the label)

1.1 Supraventricular Tachycardia or Noncompensatory Sinus Tachycardia Esmolol hydrochloride injection is indicated for the rapid control of ventricular rate in patients with atrial fibrillation or atrial flutter in perioperative, postoperative, or other emergent circumstances where short term control of ventricular rate with a short-acting agent is desirable. Esmolol hydrochloride injection is also indicated in noncompensatory sinus tachycardia where, in the physician’s judgment, the rapid heart rate requires specific intervention. Esmolol hydrochloride injection is intended for short-term use. 1.2 Intraoperative and Postoperative Tachycardia and Hypertension Esmolol hydrochloride injection …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51662-1444

What is NDC 51662-1444?
51662-1444 is the product NDC for Esmolol Hydrochloride, Esmolol hydrochloride 100 mg/10mL injection, solution, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Esmolol Hydrochloride.
What is the active ingredient?
Esmolol hydrochloride.
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 Esmolol Hydrochloride?
23 other product NDCs are listed under this name. See all Esmolol Hydrochloride 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 Esmolol Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousREMEDYREPACK INC.70518-441070518-4410-00
Esmolol HydrochlorideEsmolol hydrochloride 10 mg/mLInjection, SolutionIntravenousHenry Schein, Inc.0404-978500404-9785-10
Esmolol Hydrochlorideesmolol hydrochloride in sodium chlorideEsmolol hydrochloride 10 mg/mLInjectionIntravenousAmneal Pharmaceuticals LLC70121-171670121-1716-0370121-1716-07
Esmolol Hydrochlorideesmolol hydrochloride in sodium chlorideEsmolol hydrochloride 20 mg/mLInjectionIntravenousAmneal Pharmaceuticals LLC70121-171770121-1717-0370121-1717-07
Esmolol Hydrochlorideesmolol hydrochloride in sodium chlorideEsmolol hydrochloride 10 mg/mLInjectionIntravenousWG Critical Care, LLC44567-45044567-0450-10
Esmolol Hydrochlorideesmolol hydrochloride in sodium chlorideEsmolol hydrochloride 20 mg/mLInjectionIntravenousWG Critical Care, LLC44567-45144567-0451-10
esmolol hydrochlorideesmolol hydrochloride in sodium chlorideEsmolol hydrochloride 10 mg/mLInjectionIntravenousEugia US LLC55150-42055150-0420-10
esmolol hydrochlorideesmolol hydrochloride in sodium chlorideEsmolol hydrochloride 20 mg/mLInjectionIntravenousEugia US LLC55150-42155150-0421-10
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousHenry Schein, Inc.0404-985800404-9858-10
Esmolol HydrochlorideEsmolol hydrochloride 10 mg/mLInjectionIntravenousHF Acquisition Co LLC, DBA HealthFirst51662-142751662-1427-01

All 24 Esmolol Hydrochloride NDCs

Other NDCs under ANDA 205520

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

FDA NDC Directory listings under ANDA 205520
ProductStrengthForm · routeLabelerProduct NDC
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousHenry Schein, Inc.0404-9858
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousEugia US LLC55150-194
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousREMEDYREPACK INC.70518-4410
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousMedical Purchasing Solutions, LLC71872-7049
Esmolol HydrochlorideEsmolol hydrochloride 100 mg/10mLInjection, SolutionIntravenousProPharma Distribution84549-194

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