ketamine hydrochloride (Par Pharmaceutical Inc.)
Welcome to the PulseAid listing for the ketamine hydrochloride drug offered from Par Pharmaceutical 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: | Par Pharmaceutical Inc. |
NON-PROPRIETARY NAME: | ketamine hydrochloride |
SUBSTANCE NAME: | KETAMINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | General Anesthesia [PE],General Anesthetic [EPC] |
ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2012-06-01 |
END MARKETING DATE: | 2018-05-06 |
ketamine hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | ketamine hydrochloride from Par Pharmaceutical Inc. |
LABELER NAME: | Par Pharmaceutical Inc. |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 10(mg/mL) |
START MARKETING DATE: | 2012-06-01 |
END MARKETING DATE: | 2018-05-06 |
PRODUCT ID: | 42023-137_91a4fc07-8daa-49ce-b247-1b32ed8ee250 |
PRODUCT NDC: | 42023-137 |
APPLICATION NUMBER: | NDA016812 |
Other KETAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: