SEVOFLURANE is a Respiratory (inhalation) Liquid in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Sevoflurane.
| Product ID | 10019-653_508a95e1-5f58-4ac1-95b7-5c7506f9bf21 |
| NDC | 10019-653 |
| Product Type | Human Prescription Drug |
| Proprietary Name | SEVOFLURANE |
| Generic Name | Sevoflurane |
| Dosage Form | Liquid |
| Route of Administration | RESPIRATORY (INHALATION) |
| Marketing Start Date | 2002-07-07 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA075895 |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | SEVOFLURANE |
| Active Ingredient Strength | 250 mL/250mL |
| Pharm Classes | General Anesthesia [PE],General Anesthetic [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2002-07-07 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075895 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2002-07-07 |
| Marketing Category | ANDA |
| Application Number | ANDA075895 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-07-07 |
| Marketing End Date | 2012-08-03 |
| Ingredient | Strength |
|---|---|
| SEVOFLURANE | 250 mL/250mL |
| SPL SET ID: | 22700993-851a-48aa-941e-1d2b6b04081f |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 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 |
| 66794-022 | Sevoflurane | Sevoflurane |
| 66794-012 | Sojourn | Sevoflurane |
| 0074-4456 | Ultane | Sevoflurane |