What is NDC 55150-235?

55150-235 is the product NDC for Vecuronium Bromide, Vecuronium bromide 10 mg/1 injection, powder, lyophilized, for solution, listed with the FDA by Eugia US LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Eugia US LLC, NDC labeler code 55150. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Vecuronium Bromide?

19 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Vecuronium Bromide NDC 55150-235 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)55150-235Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55150-0235Add 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
55150-235-11	55150023511	10 VIAL in 1 CARTON (55150-235-11) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (55150-235-02)Marketed from Dec 20, 2018

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): Vecuronium Bromide
Generic name (nonproprietary): vecuronium bromide
Active ingredients: Vecuronium bromide — 10 mg/1
Dosage form: Injection, Powder, Lyophilized, For solution
Route: Intravenous
Labeler: Eugia US LLCNDC labeler code 55150
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206670
Marketing start: Dec 20, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Neuromuscular Nondepolarizing Blockade (Physiologic effect)
Identifiers: Product ID 55150-235_8442842a-8400-49a7-9167-595466563a69SPL ID 8442842a-8400-49a7-9167-595466563a69SPL set ID 387b57ce-e50e-4e03-86d9-12638242bd36RxCUI 859437UNII 7E4PHP5N1DUPC 0355150236022, 0355150235025
Pharmacologic class: Nondepolarizing Neuromuscular 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

N455150023511 followed by a unit qualifier and the quantity

Package 55150-0235-11. 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 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Vecuronium bromide for injection is indicated as an adjunct to general anesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55150-235

What is NDC 55150-235?: 55150-235 is the product NDC for Vecuronium Bromide, Vecuronium bromide 10 mg/1 injection, powder, lyophilized, for solution, listed with the FDA by Eugia US LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Vecuronium Bromide.
What is the active ingredient?: Vecuronium bromide.
Who is the labeler?: Eugia US LLC, NDC labeler code 55150. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Vecuronium Bromide?: 19 other product NDCs are listed under this name. See all Vecuronium Bromide 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 Vecuronium Bromide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Vecuronium Bromide	Vecuronium bromide 10 mg/10mL	InjectionIntravenous	Mullan Pharmaceutical Inc.	83301-0056	83301-0056-02
Vecuronium Bromide	Vecuronium bromide 20 mg/20mL	InjectionIntravenous	Mullan Pharmaceutical Inc.	83301-0057	83301-0057-02
Vecuronium Bromide	Vecuronium bromide 10 mg/10mL	Injection, Powder, Lyophilized, For solutionIntravenous	Meitheal Pharmaceuticals Inc.	71288-744	71288-0744-11
Vecuronium Bromide	Vecuronium bromide 20 mg/20mL	Injection, Powder, Lyophilized, For solutionIntravenous	Meitheal Pharmaceuticals Inc.	71288-745	71288-0745-21
Vecuronium Bromide	Vecuronium bromide 1 mg/mL	Injection, Powder, Lyophilized, For solutionIntravenous	Sagent Pharmaceuticals	25021-685	25021-0685-10
Vecuronium Bromide	Vecuronium bromide 1 mg/mL	Injection, Powder, Lyophilized, For solutionIntravenous	Sagent Pharmaceuticals	25021-686	25021-0686-20
Vecuronium Bromide	Vecuronium bromide 10 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1547	51662-1547-01
Vecuronium Bromide	Vecuronium bromide 10 mg/1	Injection, Powder, For solutionIntravenous	Phlow Corp.	81565-206	81565-0206-02
Vecuronium Bromide	Vecuronium bromide 20 mg/1	Injection, Powder, For solutionIntravenous	Hikma Pharmaceuticals USA Inc.	0143-9232	00143-9232-10
Vecuronium Bromide	Vecuronium bromide 10 mg/1	Injection, Powder, For solutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1707	51662-1707-01

All 20 Vecuronium Bromide NDCs

Other NDCs under ANDA 206670

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

FDA NDC Directory listings under ANDA 206670
Product	Strength	Form · route	Labeler	Product NDC
Vecuronium Bromide	Vecuronium bromide 20 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous	Eugia US LLC	55150-236
Vecuronium Bromide	Vecuronium bromide 20 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous	Eugia US LLC	55150-236
Vecuronium Bromide	Vecuronium bromide 10 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1547