Ultane is a Respiratory (inhalation) Liquid in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is Sevoflurane.
| Product ID | 0074-4456_048607d6-77e3-4d40-83c2-d7e0a8dfdc60 |
| NDC | 0074-4456 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Ultane |
| Generic Name | Sevoflurane |
| Dosage Form | Liquid |
| Route of Administration | RESPIRATORY (INHALATION) |
| Marketing Start Date | 1995-06-07 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020478 |
| Labeler Name | AbbVie Inc. |
| Substance Name | SEVOFLURANE |
| Active Ingredient Strength | 250 mL/250mL |
| Pharm Classes | General Anesthesia [PE], General Anesthetic [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 1995-06-07 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA020478 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-06-07 |
| Marketing Category | NDA |
| Application Number | NDA020478 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-06-07 |
| Ingredient | Strength |
|---|---|
| SEVOFLURANE | 250 mL/250mL |
| SPL SET ID: | c9aa6489-5a36-44ed-9512-b996833d82f7 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0074-4456 | Ultane | Sevoflurane |
| 0781-6160 | Sevoflurane | Sevoflurane |
| 10019-651 | Sevoflurane | Sevoflurane |
| 10019-653 | SEVOFLURANE | Sevoflurane |
| 10019-655 | Sevoflurane | Sevoflurane |
| 10019-657 | SEVOFLURANE | Sevoflurane |
| 12164-005 | Sevoflurane | sevoflurane |
| 66794-015 | Sevoflurane | Sevoflurane |
| 66794-012 | Sojourn | Sevoflurane |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTANE 74412392 1935853 Live/Registered |
ABBVIE INC. 1993-07-14 |