NDC codes

FDA NDC Directory
Product NDC (as listed)0074-4456Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00074-4456Add 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
0074-4456-0400074445604250 mL in 1 BOTTLE, PLASTIC (0074-4456-04)Marketed from Jun 7, 1995

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Ultane
Generic name (nonproprietary)
sevoflurane
Active ingredients
Sevoflurane — 250 mL/250mL
Dosage form
Liquid
Route
Respiratory (Inhalation)
Labeler
AbbVie Inc.NDC labeler code 0074
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 020478
Marketing start
Listing expires
Other FDA classes
General Anesthesia (Physiologic effect)
Identifiers
Product ID 0074-4456_20a177a4-8440-46f9-98f4-c51d395e4a46SPL ID 20a177a4-8440-46f9-98f4-c51d395e4a46SPL set ID 4c6e76bc-c964-4955-e0a3-511d3386a9ccRxCUI 200243, 541963UNII 38LVP0K73A
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.

NDC on a medical claim

N400074445604 followed by a unit qualifier and the quantity

Package 00074-4456-04. 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)

INDICATIONS AND USAGE ULTANE is indicated for induction and maintenance of general anesthesia in adult and pediatric patients for inpatient and outpatient surgery. ULTANE should be administered only by persons trained in the administration of general anesthesia. Facilities for maintenance of a patent airway, artificial ventilation, oxygen enrichment, and circulatory resuscitation must be immediately available. Since level of anesthesia may be altered rapidly, only vaporizers producing predictable concentrations of sevoflurane should be used.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0074-4456

What is NDC 0074-4456?
0074-4456 is the product NDC for Ultane (sevoflurane), Sevoflurane 250 mL/250mL liquid, listed with the FDA by AbbVie Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ultane (Sevoflurane).
What is the active ingredient?
Sevoflurane.
Who is the labeler?
AbbVie Inc., NDC labeler code 0074. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ultane?
1 other product NDC are listed under this name. See all Ultane NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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