NDC codes

FDA NDC Directory
Product NDC (as listed)67457-914Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67457-0914Add 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
67457-914-056745709140510 VIAL, GLASS in 1 CARTON (67457-914-05) / 10 mL in 1 VIAL, GLASS (67457-914-00)Marketed from Apr 15, 2020

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)
Ultiva
Generic name (nonproprietary)
remifentanil hydrochloride
Active ingredients
Remifentanil hydrochloride — 1 mg/mL
Dosage form
Injection, Powder, Lyophilized, For solution
Route
Intravenous
Labeler
Mylan Institutional LLCNDC labeler code 67457
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 020630
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 67457-914_c60a1e36-91ef-4360-92b8-79e120304b6eSPL ID c60a1e36-91ef-4360-92b8-79e120304b6eSPL set ID 4dbcb8f9-1987-4b66-bd2f-d251fda0be10RxCUI 1729578, 1729581, 1729584, 1729586, 1729710, 1729712UNII 5V444H5WIC
Pharmacologic class
Opioid Agonist

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

N467457091405 followed by a unit qualifier and the quantity

Package 67457-0914-05. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

ULTIVA is indicated for intravenous (IV) administration: • As an analgesic agent for use during the induction and maintenance of general anesthesia for inpatient and outpatient procedures. • For continuation as an analgesic into the immediate postoperative period in adult patients under the direct supervision of an anesthesia practitioner in a postoperative anesthesia care unit or intensive care setting. • As an analgesic component of monitored anesthesia care in adult patients. ULTIVA is an opioid agonist indicated for intravenous administration: • As an analgesic agent for use during the induction and maintenance of general anesthesia for inpatient and outpatient procedures. ( 1 ) • For co…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67457-914

What is NDC 67457-914?
67457-914 is the product NDC for Ultiva (remifentanil hydrochloride), Remifentanil hydrochloride 1 mg/mL injection, powder, lyophilized, for solution, listed with the FDA by Mylan Institutional LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ultiva (Remifentanil Hydrochloride).
What is the active ingredient?
Remifentanil hydrochloride.
Who is the labeler?
Mylan Institutional LLC, NDC labeler code 67457. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ultiva?
5 other product NDCs are listed under this name. See all Ultiva 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 Ultiva NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC72078-03672078-0036-05
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC72078-03572078-0035-02
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC72078-03472078-0034-01
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC67457-91267457-0912-01
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC67457-91367457-0913-02

Other NDCs under NDA 020630

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

FDA NDC Directory listings under NDA 020630
ProductStrengthForm · routeLabelerProduct NDC
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC67457-913
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC67457-912
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC72078-034
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC72078-035
Ultivaremifentanil hydrochlorideRemifentanil hydrochloride 1 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMylan Institutional LLC72078-036

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Ultiva NDC 67457-914 | National Drug Code | Med-Code