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: