Ultane (AbbVie Inc.)
Welcome to the PulseAid listing for the Ultane drug offered from AbbVie Inc.. This General Anesthesia [PE],General Anesthetic [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | AbbVie Inc. |
| NON-PROPRIETARY NAME: | Sevoflurane |
| SUBSTANCE NAME: | SEVOFLURANE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | General Anesthesia [PE],General Anesthetic [EPC] |
| ROUTE: | RESPIRATORY (INHALATION) |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1995-06-07 |
| END MARKETING DATE: | 0000-00-00 |
Ultane HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ultane from AbbVie Inc. |
| LABELER NAME: | AbbVie Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 250(mL/250mL) |
| START MARKETING DATE: | 1995-06-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0074-4456_14d52736-b223-d525-dfb2-a27c808adece |
| PRODUCT NDC: | 0074-4456 |
| APPLICATION NUMBER: | NDA020478 |
Other SEVOFLURANE Pharmaceutical Manufacturers / Labelers:
