Prescription drug · NDA
Ultane (Sevoflurane) NDC 0074-4456
Sevoflurane 250 mL/250mL · Liquid · Respiratory (Inhalation) · AbbVie Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0074-4456-04 | 00074445604 | 250 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
N400074445604followed by a unit qualifier and the quantityPackage 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.
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.