Ketalar (Par Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Ketalar 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 |
| START MARKETING DATE: | 2007-10-01 |
| END MARKETING DATE: | 0000-00-00 |
Ketalar HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ketalar from Par Pharmaceutical, Inc. |
| LABELER NAME: | Par Pharmaceutical, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2007-10-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 42023-113_b94ace1b-96b4-4ef9-8632-06e868a2049b |
| PRODUCT NDC: | 42023-113 |
| APPLICATION NUMBER: | NDA016812 |
Other KETAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
