What is NDC 72485-508?

72485-508 is the product NDC for Etomidate, Etomidate 2 mg/mL injection, solution, listed with the FDA by Armas Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Armas Pharmaceuticals Inc., NDC labeler code 72485. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Etomidate?

21 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Etomidate NDC 72485-508 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72485-508Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72485-0508Add 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
72485-508-10	7248505081072485050810	10 VIAL, SINGLE-DOSE in 1 CARTON (72485-508-10) / 10 mL in 1 VIAL, SINGLE-DOSE (72485-508-01)Marketed from Jan 22, 2024

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): Etomidate
Generic name (nonproprietary): etomidate
Active ingredients: Etomidate — 2 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Armas Pharmaceuticals Inc.NDC labeler code 72485
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215028
Marketing start: Jan 22, 2024
Listing expires: Dec 31, 2026
Other FDA classes: General Anesthesia (Physiologic effect)
Identifiers: Product ID 72485-508_7444860b-36c1-459d-94ba-d7301d9dc2caSPL ID 7444860b-36c1-459d-94ba-d7301d9dc2caSPL set ID 75467058-da52-48fa-8d4e-e1025ec7d461RxCUI 1654006, 1654008UNII Z22628B598UPC 0372485508013
Pharmacologic class: General Anesthetic

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

N472485050810 followed by a unit qualifier and the quantity

Package 72485-0508-10. 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 Jan 22, 2024.

Indications (excerpt from the label)

INDICATIONS & USAGE Etomidate Injection USP is indicated by intravenous injection for the induction of general anesthesia. When considering use of etomidate, the usefulness of its hemodynamic properties (see CLINICAL PHARMACOLOGY ) should be weighed against the high frequency of transient skeletal muscle movements (see ADVERSE REACTIONS ). Intravenous etomidate is also indicated for the supplementation of subpotent anesthetic agents, such as nitrous oxide in oxygen, during maintenance of anesthesia for short operative procedures such as dilation and curettage or cervical conization.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72485-508

What is NDC 72485-508?: 72485-508 is the product NDC for Etomidate, Etomidate 2 mg/mL injection, solution, listed with the FDA by Armas Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Etomidate.
What is the active ingredient?: Etomidate.
Who is the labeler?: Armas Pharmaceuticals Inc., NDC labeler code 72485. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Etomidate?: 21 other product NDCs are listed under this name. See all Etomidate 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 Etomidate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Caplin Steriles Limited	65145-127	65145-0127-10
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Caplin Steriles Limited	65145-128	65145-0128-10
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Armas Pharmaceuticals Inc.	72485-509	72485-0509-10
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Fresenius Kabi USA, LLC	65219-445	65219-0445-22
Etomidate	Etomidate 40 mg/20mL	Injection, SolutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1542	51662-1542-01
Etomidate	Etomidate 2 mg/mL	InjectionIntravenous	Civica, Inc.	72572-160	72572-0160-10
Etomidate	Etomidate 2 mg/mL	InjectionIntravenous	Civica, Inc.	72572-161	72572-0161-10
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Fresenius Kabi USA, LLC	65219-447	65219-0447-20
Etomidate	Etomidate 2 mg/mL	InjectionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1485	51662-1485-01
Etomidateetomidate injection	Etomidate 2 mg/mL	SolutionIntravenous	Fosun Pharma USA Inc	72266-146	72266-0146-10

All 22 Etomidate NDCs

Other NDCs under ANDA 215028

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

FDA NDC Directory listings under ANDA 215028
Product	Strength	Form · route	Labeler	Product NDC
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Caplin Steriles Limited	65145-127
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Caplin Steriles Limited	65145-128
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Fresenius Kabi USA, LLC	65219-445
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Fresenius Kabi USA, LLC	65219-447
Etomidate	Etomidate 2 mg/mL	Injection, SolutionIntravenous	Armas Pharmaceuticals Inc.	72485-509